{"id":16019,"date":"2023-03-30T16:52:31","date_gmt":"2023-03-30T14:52:31","guid":{"rendered":"https:\/\/genomik-tuebingen.de\/?page_id=16019"},"modified":"2026-01-09T11:13:12","modified_gmt":"2026-01-09T10:13:12","slug":"einzelgen-und-segregationsanalyse","status":"publish","type":"page","link":"https:\/\/cegat.com\/de\/diagnostik\/einzelgen-und-segregationsanalyse\/","title":{"rendered":"Einzelgen- und Segregationsanalyse"},"content":{"rendered":"<p><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-1 fusion-flex-container has-pattern-background has-mask-background fusion-parallax-none hundred-percent-fullwidth non-hundred-percent-height-scrolling lazyload\" style=\"--awb-background-position:center top;--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-padding-top-small:60px;--awb-padding-bottom-small:60px;--awb-margin-top:-60px;--awb-min-height:500px;--awb-background-size:cover;--awb-flex-wrap:wrap;\" data-bg=\"https:\/\/cegat.com\/wp-content\/uploads\/2022\/08\/cegat_kv_einzelgen_panel.png\" ><\/div><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-2 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-padding-bottom-small:0px;--awb-margin-bottom-small:0px;--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"max-width:1248px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-0 fusion_builder_column_3_4 3_4 fusion-flex-column fusion-animated\" style=\"--awb-padding-right:20px;--awb-padding-bottom:80px;--awb-padding-left:20px;--awb-padding-right-small:10px;--awb-padding-bottom-small:50px;--awb-padding-left-small:10px;--awb-overflow:hidden;--awb-bg-color:rgba(255,255,255,0.75);--awb-bg-color-hover:rgba(255,255,255,0.75);--awb-bg-size:cover;--awb-border-color:rgba(255,255,255,0);--awb-border-top:1px;--awb-border-right:1px;--awb-border-bottom:1px;--awb-border-left:1px;--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:75%;--awb-margin-top-large:-145px;--awb-spacing-right-large:0px;--awb-margin-bottom-large:20px;--awb-spacing-left-large:0px;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:0px;--awb-spacing-left-medium:0px;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:0px;--awb-spacing-left-small:0px;\" data-animationType=\"fadeInUp\" data-animationDuration=\"1.5\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-1 fusion-sep-none fusion-title-text fusion-title-size-one\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-bottom:0px;--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h1 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:46;line-height:var(--awb-typography1-line-height);\">Einzelgen- und Segregationsanalyse<\/h1><\/div><div class=\"fusion-text fusion-text-1\" style=\"--awb-font-size:24px;--awb-line-height:1.2;\"><p style=\"text-align: left; font-weight: 300;\">Zur fokussierten Untersuchung einzelner Gene oder famili\u00e4rer Varianten<\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-1 fusion_builder_column_1_4 1_4 fusion-flex-column fusion-no-small-visibility fusion-no-medium-visibility\" style=\"--awb-bg-size:cover;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><\/div><\/div><\/div><\/div><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-3 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--link_hover_color: var(--awb-color3);--link_color: var(--awb-color1);--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-padding-bottom:60px;--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"max-width:1248px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-2 fusion_builder_column_1_1 1_1 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><nav class=\"fusion-breadcrumbs awb-yoast-breadcrumbs fusion-breadcrumbs-1\" style=\"--awb-text-color:var(--awb-custom_color_1);--awb-breadcrumb-sep:&#039;\/&#039;;\" aria-label=\"Breadcrumb\"><ol class=\"awb-breadcrumb-list\"><li class=\"fusion-breadcrumb-item awb-breadcrumb-sep awb-home\" ><a href=\"https:\/\/cegat.com\/de\/\" class=\"fusion-breadcrumb-link\"><span >Home<\/span><\/a><\/li><\/ol><\/nav>\n<\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-3 fusion_builder_column_3_4 3_4 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:75%;--awb-margin-top-large:0px;--awb-spacing-right-large:2.56%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:2.56%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-text fusion-text-2\"><p style=\"text-align: justify;\">CeGaT bietet, mit mehr als 700 verschiedenen Einzelgen-Sequenzanalysen, eine sehr umfassende Labordiagnostik an. Weiterhin f\u00fchren wir f\u00fcr viele dieser Gene (&gt; 350) Untersuchungen auf Deletionen und Duplikationen mittels MLPA oder quantitativer PCR durch.<\/p>\n<p style=\"text-align: justify;\">Da immer mehr Erkrankungen molekulargenetisch diagnostizierbar sind, erweitern wir das Spektrum unserer Diagnostiken st\u00e4ndig. Wir sind gern bereit, f\u00fcr Sie neue Untersuchungen zu etablieren.<\/p>\n<p style=\"text-align: justify;\">Sie sind in Deutschland versichert? Unsere Kolleginnen und Kollegen vom <a href=\"https:\/\/www.humangenetik-tuebingen.de\/\" target=\"_blank\" rel=\"noopener\">Zentrum f\u00fcr Humangenetik T\u00fcbingen<\/a> beraten Sie gerne!<\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-4 fusion_builder_column_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:7.68%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-0 fusion_builder_column_inner_1_1 1_1 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div ><a class=\"fusion-button button-flat fusion-button-default-size button-custom fusion-button-default button-1 fusion-button-span-yes fusion-button-default-type\" style=\"--awb-margin-top:10px;--awb-margin-bottom:10px;--button_accent_color:var(--awb-color1);--button_border_color:var(--awb-color1);--button_accent_hover_color:var(--awb-color5);--button_border_hover_color:rgba(255,255,255,0);--button_border_width-top:1px;--button_border_width-right:1px;--button_border_width-bottom:1px;--button_border_width-left:1px;--button_gradient_top_color:rgba(255,255,255,0);--button_gradient_bottom_color:rgba(255,255,255,0);--button_gradient_top_color_hover:var(--awb-color1);--button_gradient_bottom_color_hover:var(--awb-color1);\" target=\"_self\" href=\"#tabelle\"><span class=\"fusion-button-text awb-button__text awb-button__text--default\">Zur Einzelgen-\u00dcbersicht<\/span><\/a><\/div><div ><a class=\"fusion-button button-flat fusion-button-default-size button-custom fusion-button-default button-2 fusion-button-span-yes fusion-button-default-type\" style=\"--awb-margin-top:10px;--awb-margin-bottom:10px;--button_accent_color:var(--awb-color1);--button_border_color:var(--awb-color1);--button_accent_hover_color:var(--awb-color5);--button_border_hover_color:rgba(255,255,255,0);--button_border_width-top:1px;--button_border_width-right:1px;--button_border_width-bottom:1px;--button_border_width-left:1px;--button_gradient_top_color:rgba(255,255,255,0);--button_gradient_bottom_color:rgba(255,255,255,0);--button_gradient_top_color_hover:var(--awb-color1);--button_gradient_bottom_color_hover:var(--awb-color1);\" target=\"_self\" href=\"#download\"><span class=\"fusion-button-text awb-button__text awb-button__text--default\">Einsendeformulare<\/span><\/a><\/div><div ><a class=\"fusion-button button-flat fusion-button-default-size button-custom fusion-button-default button-3 fusion-button-span-yes fusion-button-default-type fusion-no-small-visibility\" style=\"--awb-margin-top:10px;--awb-margin-bottom:10px;--button_accent_color:var(--awb-color1);--button_border_color:var(--awb-color1);--button_accent_hover_color:var(--awb-color5);--button_border_hover_color:rgba(255,255,255,0);--button_border_width-top:1px;--button_border_width-right:1px;--button_border_width-bottom:1px;--button_border_width-left:1px;--button_gradient_top_color:rgba(255,255,255,0);--button_gradient_bottom_color:rgba(255,255,255,0);--button_gradient_top_color_hover:var(--awb-color1);--button_gradient_bottom_color_hover:var(--awb-color1);\" target=\"_self\" href=\"#\" data-toggle=\"modal\" data-target=\".fusion-modal.portal_EG\"><span class=\"fusion-button-text awb-button__text awb-button__text--default\">Jetzt bestellen<\/span><\/a><\/div><div class=\"fusion-modal modal fade modal-1 portal_EG\" tabindex=\"-1\" role=\"dialog\" aria-labelledby=\"modal-heading-1\" aria-hidden=\"true\" style=\"--awb-border-color:var(--awb-color5);--awb-background:var(--awb-color5);\"><div class=\"modal-dialog modal-lg\" role=\"document\"><div class=\"modal-content fusion-modal-content\"><div class=\"modal-header\"><button class=\"close\" type=\"button\" data-dismiss=\"modal\" aria-hidden=\"true\" aria-label=\"Close\">&times;<\/button><h3 class=\"modal-title\" id=\"modal-heading-1\" data-dismiss=\"modal\" aria-hidden=\"true\"><\/h3><\/div><div class=\"modal-body fusion-clearfix\">\n<p>Bitte ausw\u00e4hlen:<\/p>\n<div class=\"fusion-button-wrapper fusion-align-block\"><a class=\"fusion-button button-flat fusion-button-default-size button-custom fusion-button-default button-4 fusion-button-span-yes fusion-button-default-type\" style=\"--awb-margin-bottom:10px;--awb-padding-top:20px;--awb-padding-bottom:20px;--button_accent_color:var(--awb-color1);--button_border_color:var(--awb-color1);--button_accent_hover_color:var(--awb-color5);--button_border_hover_color:rgba(255,255,255,0);--button_border_width-top:1px;--button_border_width-right:1px;--button_border_width-bottom:1px;--button_border_width-left:1px;--button_gradient_top_color:rgba(255,255,255,0);--button_gradient_bottom_color:rgba(255,255,255,0);--button_gradient_top_color_hover:var(--awb-color1);--button_gradient_bottom_color_hover:var(--awb-color1);\" target=\"_self\" href=\"https:\/\/my.cegat.de\/?_lang=de#\/order\/new\/form-0bc2d8bb-acbe-4b83-b92c-1010bac8715b\/\"><span class=\"fusion-button-text awb-button__text awb-button__text--default\">Jetzt molekulargenetische Diagnostik bestellen<\/span><\/a><\/div>\n<div class=\"fusion-button-wrapper fusion-align-block\"><a class=\"fusion-button button-flat fusion-button-default-size button-custom fusion-button-default button-5 fusion-button-span-yes fusion-button-default-type\" style=\"--awb-padding-top:20px;--awb-padding-bottom:20px;--button_accent_color:var(--awb-color1);--button_border_color:var(--awb-color1);--button_accent_hover_color:var(--awb-color5);--button_border_hover_color:rgba(255,255,255,0);--button_border_width-top:1px;--button_border_width-right:1px;--button_border_width-bottom:1px;--button_border_width-left:1px;--button_gradient_top_color:rgba(255,255,255,0);--button_gradient_bottom_color:rgba(255,255,255,0);--button_gradient_top_color_hover:var(--awb-color1);--button_gradient_bottom_color_hover:var(--awb-color1);\" target=\"_self\" href=\"https:\/\/my.cegat.de\/?_lang=de#\/order\/new\/form-264a6795-7d17-4efb-8382-c0509c4e6dc2\/\"><span class=\"fusion-button-text awb-button__text awb-button__text--default\">Jetzt Familienanalyse (Segregationsanalyse) bestellen<\/span><\/a><\/div>\n<\/div><\/div><\/div><\/div><div ><a class=\"fusion-button button-flat fusion-button-default-size button-custom fusion-button-default button-6 fusion-button-span-yes fusion-button-default-type\" style=\"--awb-margin-top:10px;--awb-margin-bottom:10px;--button_accent_color:var(--awb-color1);--button_border_color:var(--awb-color1);--button_accent_hover_color:var(--awb-color5);--button_border_hover_color:rgba(255,255,255,0);--button_border_width-top:1px;--button_border_width-right:1px;--button_border_width-bottom:1px;--button_border_width-left:1px;--button_gradient_top_color:rgba(255,255,255,0);--button_gradient_bottom_color:rgba(255,255,255,0);--button_gradient_top_color_hover:var(--awb-color1);--button_gradient_bottom_color_hover:var(--awb-color1);\" target=\"_self\" href=\"#kontakt-form\"><span class=\"fusion-button-text awb-button__text awb-button__text--default\">Kontaktieren Sie uns<\/span><\/a><\/div><\/div><\/div><\/div><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-1 fusion_builder_column_inner_1_2 1_2 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:10%;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:25%;--awb-order-medium:0;--awb-margin-top-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:50%;--awb-order-small:0;--awb-margin-top-small:0;--awb-spacing-right-small:3.84%;--awb-spacing-left-small:3.84%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element sm-text-align-center\" style=\"--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-1 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"144\" height=\"80\" alt=\"DAkkS Logo Diagnostik\" title=\"DAkkS_Symbol_Diagnostik\" src=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27144%27%20height%3D%2780%27%20viewBox%3D%270%200%20144%2080%27%3E%3Crect%20width%3D%27144%27%20height%3D%2780%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2022\/07\/DAkkS_Symbol_Diagnostik.jpg\" class=\"lazyload img-responsive wp-image-34497\"\/><\/span><\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-2 fusion_builder_column_inner_1_2 1_2 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:10%;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:25%;--awb-order-medium:0;--awb-margin-top-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:50%;--awb-order-small:0;--awb-margin-top-small:0;--awb-spacing-right-small:3.84%;--awb-spacing-left-small:3.84%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element sm-text-align-center\" style=\"--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-2 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"123\" height=\"80\" alt=\"CAP CLIA Zertifizierung\" title=\"Logo_CAP\" src=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27123%27%20height%3D%2780%27%20viewBox%3D%270%200%20123%2080%27%3E%3Crect%20width%3D%27123%27%20height%3D%2780%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2022\/07\/Logo_CAP.jpg\" class=\"lazyload img-responsive wp-image-34495\"\/><\/span><\/div><\/div><\/div><\/div>\n<\/div><\/div><\/div><\/div><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-4 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-padding-top:60px;--awb-padding-bottom:60px;--awb-background-color:rgba(41,65,144,0.05);--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"max-width:1248px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-5 fusion_builder_column_1_1 1_1 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-margin-bottom-medium:0;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-2 fusion-sep-none fusion-title-text fusion-title-size-two\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h2 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:36;line-height:var(--awb-typography1-line-height);\">Was wir Ihnen mit der Einzelgen-Diagnostik bieten<\/h2><\/div><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-3 fusion_builder_column_inner_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-padding-top:40px;--awb-padding-right:20px;--awb-padding-bottom:40px;--awb-padding-left:20px;--awb-overflow:hidden;--awb-bg-color:var(--awb-color5);--awb-bg-color-hover:var(--awb-color5);--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-3 fusion-sep-none fusion-title-center fusion-title-text fusion-title-size-four\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h4 class=\"fusion-title-heading title-heading-center fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:24;--minFontSize:24;line-height:var(--awb-typography1-line-height);\">Umfangreiche Diagnostik<\/h4><\/div><div class=\"fusion-text fusion-text-3\"><p style=\"text-align: center;\">&gt; 700 verschiedene Einzelgen-Sequenzanalysen<\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-4 fusion_builder_column_inner_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-padding-top:40px;--awb-padding-right:20px;--awb-padding-bottom:40px;--awb-padding-left:20px;--awb-overflow:hidden;--awb-bg-color:var(--awb-color5);--awb-bg-color-hover:var(--awb-color5);--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-4 fusion-sep-none fusion-title-center fusion-title-text fusion-title-size-four\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h4 class=\"fusion-title-heading title-heading-center fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:24;--minFontSize:24;line-height:var(--awb-typography1-line-height);\">Deletionen &amp; Duplikationen<\/h4><\/div><div class=\"fusion-text fusion-text-4\"><p style=\"text-align: center;\">Mittels MLPA oder quantitativer PCR in &gt; 350 Genen<\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-5 fusion_builder_column_inner_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-padding-top:40px;--awb-padding-right:20px;--awb-padding-bottom:40px;--awb-padding-left:20px;--awb-overflow:hidden;--awb-bg-color:var(--awb-color5);--awb-bg-color-hover:var(--awb-color5);--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-margin-bottom-small:20px;--awb-spacing-left-small:1.92%;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-5 fusion-sep-none fusion-title-center fusion-title-text fusion-title-size-four\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h4 class=\"fusion-title-heading title-heading-center fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:24;--minFontSize:24;line-height:var(--awb-typography1-line-height);\">Hohe<br \/>\nFlexibilit\u00e4t<\/h4><\/div><div class=\"fusion-text fusion-text-5\"><p style=\"text-align: center;\">Wir sind gern bereit, f\u00fcr Sie neue Untersuchungen zu etablieren<\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-6 fusion_builder_column_inner_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-padding-top:40px;--awb-padding-right:20px;--awb-padding-bottom:40px;--awb-padding-left:20px;--awb-overflow:hidden;--awb-bg-color:var(--awb-color5);--awb-bg-color-hover:var(--awb-color5);--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-6 fusion-sep-none fusion-title-center fusion-title-text fusion-title-size-four\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h4 class=\"fusion-title-heading title-heading-center fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:24;--minFontSize:24;line-height:var(--awb-typography1-line-height);\">Medizinischer<br \/>\nBefund<\/h4><\/div><div class=\"fusion-text fusion-text-6\"><p style=\"text-align: center;\">Erstellt von unserem interdisziplin\u00e4ren Expertenteam<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-5 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-padding-top:60px;--awb-padding-bottom:60px;--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"max-width:1248px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-6 fusion_builder_column_1_1 1_1 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-7 fusion-sep-none fusion-title-text fusion-title-size-two\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h2 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:36;line-height:var(--awb-typography1-line-height);\">Unser Versprechen an Sie<\/h2><\/div><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-7 fusion_builder_column_inner_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-padding-right:20px;--awb-padding-left:20px;--awb-overflow:hidden;--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:50%;--awb-order-small:0;--awb-spacing-right-small:3.84%;--awb-spacing-left-small:3.84%;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element \" style=\"text-align:center;--awb-max-width:30%;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-3 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"80\" height=\"80\" alt=\"Icon zur Visualisierung der Dauer\" title=\"cegat_icon_Dauer\" src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_Dauer.png\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_Dauer-80x80.png\" class=\"lazyload img-responsive wp-image-38878\" srcset=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27300%27%20viewBox%3D%270%200%20300%20300%27%3E%3Crect%20width%3D%27300%27%20height%3D%27300%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-srcset=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_Dauer-200x200.png 200w, https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_Dauer.png 300w\" data-sizes=\"auto\" data-orig-sizes=\"(max-width: 768px) 100vw, 80px\" \/><\/span><\/div><div class=\"fusion-title title fusion-title-8 fusion-sep-none fusion-title-center fusion-title-text fusion-title-size-four\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h4 class=\"fusion-title-heading title-heading-center fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:24;--minFontSize:24;line-height:var(--awb-typography1-line-height);\">Schnelle Bearbeitung<\/h4><\/div><div class=\"fusion-text fusion-text-7\"><p style=\"text-align: center;\">&lt; Vier Wochen nach Probeneingang<\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-8 fusion_builder_column_inner_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-padding-right:20px;--awb-padding-left:20px;--awb-overflow:hidden;--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:50%;--awb-order-small:0;--awb-spacing-right-small:3.84%;--awb-spacing-left-small:3.84%;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element \" style=\"text-align:center;--awb-max-width:30%;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-4 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"80\" height=\"80\" alt=\"Icon zur Visualisierung unseres Sicherheitsversprechens\" title=\"cegat_Icon_Sicherheit_grau\" src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_Icon_Sicherheit_grau.png\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_Icon_Sicherheit_grau-80x80.png\" class=\"lazyload img-responsive wp-image-38910\" srcset=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27300%27%20viewBox%3D%270%200%20300%20300%27%3E%3Crect%20width%3D%27300%27%20height%3D%27300%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-srcset=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_Icon_Sicherheit_grau-200x200.png 200w, https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_Icon_Sicherheit_grau.png 300w\" data-sizes=\"auto\" data-orig-sizes=\"(max-width: 768px) 100vw, 80px\" \/><\/span><\/div><div class=\"fusion-title title fusion-title-9 fusion-sep-none fusion-title-center fusion-title-text fusion-title-size-four\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h4 class=\"fusion-title-heading title-heading-center fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:24;--minFontSize:24;line-height:var(--awb-typography1-line-height);\">Sicherheit<\/h4><\/div><div class=\"fusion-text fusion-text-8\"><p style=\"text-align: center;\">H\u00f6chste Vertraulichkeit und Qualit\u00e4tsstandards<\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-9 fusion_builder_column_inner_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-padding-right:20px;--awb-padding-left:20px;--awb-overflow:hidden;--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:50%;--awb-order-small:0;--awb-spacing-right-small:3.84%;--awb-margin-bottom-small:20px;--awb-spacing-left-small:3.84%;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element \" style=\"text-align:center;--awb-max-width:30%;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-5 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"80\" height=\"80\" alt=\"Icon das Zuverl\u00e4ssigkeit symbolisiert\" title=\"cegat_Icon_Zuverl\u00e4ssig\" src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_Icon_Zuverlaessig.png\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_Icon_Zuverlaessig-80x80.png\" class=\"lazyload img-responsive wp-image-35023\" srcset=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27300%27%20viewBox%3D%270%200%20300%20300%27%3E%3Crect%20width%3D%27300%27%20height%3D%27300%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-srcset=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_Icon_Zuverlaessig-200x200.png 200w, https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_Icon_Zuverlaessig.png 300w\" data-sizes=\"auto\" data-orig-sizes=\"(max-width: 768px) 100vw, 80px\" \/><\/span><\/div><div class=\"fusion-title title fusion-title-10 fusion-sep-none fusion-title-center fusion-title-text fusion-title-size-four\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h4 class=\"fusion-title-heading title-heading-center fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:24;--minFontSize:24;line-height:var(--awb-typography1-line-height);\">Zuverl\u00e4ssigkeit<\/h4><\/div><div class=\"fusion-text fusion-text-9\"><p style=\"text-align: center;\">Rundum Betreuung bei jedem Schritt<\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-10 fusion_builder_column_inner_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-padding-right:20px;--awb-padding-left:20px;--awb-overflow:hidden;--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:50%;--awb-order-small:0;--awb-spacing-right-small:3.84%;--awb-spacing-left-small:3.84%;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element \" style=\"text-align:center;--awb-max-width:30%;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-6 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"80\" height=\"80\" alt=\"Sehr vereinfachte grafische Darstellung eines Befund\" title=\"Befund_neutral\" src=\"https:\/\/cegat.com\/wp-content\/uploads\/2022\/09\/Befund_neutral.png\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2022\/09\/Befund_neutral-80x80.png\" class=\"lazyload img-responsive wp-image-37166\" srcset=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27300%27%20viewBox%3D%270%200%20300%20300%27%3E%3Crect%20width%3D%27300%27%20height%3D%27300%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-srcset=\"https:\/\/cegat.com\/wp-content\/uploads\/2022\/09\/Befund_neutral-200x200.png 200w, https:\/\/cegat.com\/wp-content\/uploads\/2022\/09\/Befund_neutral.png 300w\" data-sizes=\"auto\" data-orig-sizes=\"(max-width: 768px) 100vw, 80px\" \/><\/span><\/div><div class=\"fusion-title title fusion-title-11 fusion-sep-none fusion-title-center fusion-title-text fusion-title-size-four\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h4 class=\"fusion-title-heading title-heading-center fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:24;--minFontSize:24;line-height:var(--awb-typography1-line-height);\">Verst\u00e4ndlichkeit<\/h4><\/div><div class=\"fusion-text fusion-text-10\"><p style=\"text-align: center;\">Verst\u00e4ndlich und \u00fcbersichtlich aufbereiteter medizinischer Befund<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-6 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--link_hover_color: var(--awb-color3);--link_color: var(--awb-color1);--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-padding-top:60px;--awb-padding-bottom:60px;--awb-background-color:rgba(41,65,144,0.05);--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"max-width:1248px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-7 fusion_builder_column_1_2 1_2 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:3.84%;--awb-width-medium:50%;--awb-order-medium:0;--awb-spacing-right-medium:3.84%;--awb-spacing-left-medium:3.84%;--awb-width-small:100%;--awb-order-small:1;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-12 fusion-sep-none fusion-title-text fusion-title-size-two\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h2 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:36;line-height:var(--awb-typography1-line-height);\">Unsere Methoden<\/h2><\/div><div class=\"fusion-title title fusion-title-13 fusion-sep-none fusion-title-text fusion-title-size-three\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h3 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:28;line-height:var(--awb-typography1-line-height);\">Sanger-Sequenzierung<\/h3><\/div><div class=\"fusion-text fusion-text-11\"><p style=\"text-align: justify;\">Die direkte Sequenzanalyse mittels Kettenabbruch nach Sanger geh\u00f6rt zu den Standardmethoden in der molekulargenetischen Diagnostik. Diese Methode ist besonders sinnvoll bei der Analyse kleinerer Gene oder Genbereiche wie z. B. Hot-Spot-Mutationen und wird daher vorwiegend bei der Einzelgen-Diagnostik verwendet. Die Analyse erfolgt bei uns durch das 96-Kapillar-Sequenzierger\u00e4t 3730xl DNA Analyzer von Applied Biosystems.<\/p>\n<\/div><div class=\"fusion-title title fusion-title-14 fusion-sep-none fusion-title-text fusion-title-size-three\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h3 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:28;line-height:var(--awb-typography1-line-height);\">Deletions- und Duplikationsanalyse<\/h3><\/div><div class=\"fusion-text fusion-text-12\"><p style=\"text-align: justify;\">Zur Detektion von Deletionen oder Duplikationen werden entweder MLPA oder quantitative real-time PCR-Analysen durchgef\u00fchrt. F\u00fcr MLPAs werden die Kits von <a href=\"http:\/\/www.mlpa.com\/\" target=\"_blank\" rel=\"noopener\">MRC HOLLAND<\/a> verwendet. F\u00fcr die quantitative Real-Time PCR wird das QuantStudio\u2122 112K Flex Real-Time-PCR-System von Applied Biosystems verwendet.<\/p>\n<\/div><div class=\"fusion-title title fusion-title-15 fusion-sep-none fusion-title-text fusion-title-size-three\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h3 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:28;line-height:var(--awb-typography1-line-height);\">Fragmentl\u00e4ngenanalyse<\/h3><\/div><div class=\"fusion-text fusion-text-13\"><p style=\"text-align: justify;\">Eine weitere Methode, die bei uns Anwendung findet, ist die Fragmentl\u00e4ngenanalyse mittels Kapillarelektrophorese. Diese wird z. B. bei Triplett-Repeat-Erkrankungen durchgef\u00fchrt. Der Bereich der zu untersuchenden Genregion wird mit speziellen Primern amplifiziert, wobei durch die entstehende Fragmentl\u00e4nge der PCR-Produkte die Anzahl der Triplett-Repeats bestimmt werden kann. Die Analyse der Fragmentl\u00e4nge wird bei uns mit Hilfe des 96-Kapillar-Sequenzierger\u00e4ts 3730xl DNA Analyzer von Applied Biosystems durchgef\u00fchrt.<\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-8 fusion_builder_column_1_2 1_2 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:50%;--awb-order-medium:0;--awb-spacing-right-medium:3.84%;--awb-spacing-left-medium:3.84%;--awb-width-small:100%;--awb-order-small:3;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-16 fusion-sep-none fusion-title-text fusion-title-size-two\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h2 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:36;line-height:var(--awb-typography1-line-height);\">Beispielbefund<\/h2><\/div><div class=\"df-element dvcss dvcss_e_eyJzb3VyY2UiOiJcL3dwLWNvbnRlbnRcL3VwbG9hZHNcLzIwMjNcLzAzXC9DZUdhVF9TYW1wbGVfUmVwb3J0X1NlZ3JlZ2F0aW9uX0FuYWx5c2lzLnBkZiIsInBkZlRodW1iIjoiXC93cC1jb250ZW50XC91cGxvYWRzXC9kZWFycGRmLXRodW1ic1wvMTYwMTEuanBlZyIsImF1dG9PcGVuT3V0bGluZSI6ZmFsc2UsImF1dG9PcGVuVGh1bWJuYWlsIjpmYWxzZSwic2x1ZyI6IjE2MDExIiwiaWQiOjE2MDExLCJsaWdodGJveCI6Im5vbmUifQ==  \"><\/div><script class=\"df-shortcode-script\" type=\"application\/javascript\">if(window.DEARPDF && window.DEARPDF.parseElements){window.DEARPDF.parseElements();}<\/script><\/div><\/div><\/div><\/div><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-7 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--link_hover_color: var(--awb-color1);--link_color: var(--awb-color3);--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-padding-top:60px;--awb-padding-bottom:60px;--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"max-width:1248px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-9 fusion_builder_column_1_1 1_1 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-17 fusion-sep-none fusion-title-text fusion-title-size-two\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h2 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:36;line-height:var(--awb-typography1-line-height);\">Allgemeine Informationen<\/h2><\/div><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-11 fusion_builder_column_inner_1_2 1_2 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:50%;--awb-order-medium:0;--awb-spacing-right-medium:3.84%;--awb-spacing-left-medium:3.84%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-18 fusion-sep-none fusion-title-text fusion-title-size-three\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-bottom:-10px;--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h3 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:28;line-height:var(--awb-typography1-line-height);\">Material<\/h3><\/div><div class=\"fusion-text fusion-text-14\"><ul>\n<li>1-2 ml EDTA-Blut (empfohlene Probenart), oder<\/li>\n<li>1-2 \u00b5g genomische DNA<\/li>\n<li>CeGaT-Einsendeformular inkl. schriftliche Einverst\u00e4ndniserkl\u00e4rung nach GenDG<\/li>\n<\/ul>\n<p><a href=\"https:\/\/cegat.com\/de\/diagnostik\/allgemeine-informationen\/probenversand\/\" target=\"_blank\" rel=\"noopener\">Hier<\/a> finden Sie weitere Informationen zum sicheren Versand Ihrer Probe.<\/p>\n<\/div><div class=\"fusion-title title fusion-title-19 fusion-sep-none fusion-title-text fusion-title-size-three\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-bottom:-10px;--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h3 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:28;line-height:var(--awb-typography1-line-height);\">Dauer<\/h3><\/div><div class=\"fusion-text fusion-text-15\"><ul>\n<li>Dauer der Untersuchung: weniger als vier Wochen<\/li>\n<\/ul>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-12 fusion_builder_column_inner_1_2 1_2 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:50%;--awb-order-medium:0;--awb-spacing-right-medium:3.84%;--awb-spacing-left-medium:3.84%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-20 fusion-sep-none fusion-title-text fusion-title-size-three\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h3 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:28;line-height:var(--awb-typography1-line-height);\">Kosten<\/h3><\/div><div class=\"fusion-text fusion-text-16\"><p style=\"text-align: justify;\">Bei der Einzelgenanalyse spielt au\u00dferdem die Gr\u00f6\u00dfe bzw. die Anzahl der Exons des gew\u00fcnschten Gens eine Rolle. Neben der Sequenzierung und der bioinformatischen Analyse ist auch die Erstellung eines medizinischen Befundes durch unser Expertenteam, bestehend aus Humangenetikerinnen und\u00a0 Humangenetikern sowie Diagnostikerinnen und Diagnostikern, im Preis enthalten.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-8 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--link_hover_color: var(--awb-color1);--link_color: var(--awb-color3);--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-padding-top:60px;--awb-padding-bottom:60px;--awb-background-color:rgba(29,66,137,0.04);--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"max-width:1248px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-10 fusion_builder_column_1_2 1_2 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:3.84%;--awb-width-medium:50%;--awb-order-medium:0;--awb-spacing-right-medium:3.84%;--awb-spacing-left-medium:3.84%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-21 fusion-sep-none fusion-title-text fusion-title-size-two\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h2 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:36;line-height:var(--awb-typography1-line-height);\">Diagnostikablauf<\/h2><\/div><div class=\"fusion-separator fusion-no-small-visibility fusion-full-width-sep\" style=\"align-self: center;margin-left: auto;margin-right: auto;margin-bottom:5px;width:100%;\"><\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-11 fusion_builder_column_1_2 1_2 fusion-flex-column fusion-flex-align-self-stretch fusion-no-small-visibility\" style=\"--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:3.84%;--awb-width-medium:50%;--awb-order-medium:0;--awb-spacing-right-medium:3.84%;--awb-spacing-left-medium:3.84%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-end fusion-content-layout-column\"><div class=\"fusion-text fusion-text-17 fusion-text-no-margin\" style=\"--awb-font-size:24px;--awb-margin-bottom:10px;\"><p style=\"text-align: right; font-weight: 300;\"><a href=\"\/de\/diagnostik\/allgemeine-informationen\/probenversand\/\" target=\"_blank\" rel=\"noopener\">Hier finden Sie den gesamten Diagnostikablauf<\/a><\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-12 fusion_builder_column_1_2 1_2 fusion-flex-column fusion-flex-align-self-stretch fusion-no-medium-visibility fusion-no-large-visibility\" style=\"--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:50%;--awb-order-medium:0;--awb-spacing-right-medium:3.84%;--awb-spacing-left-medium:3.84%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-end fusion-content-layout-column\"><div class=\"fusion-text fusion-text-18 fusion-text-no-margin\" style=\"--awb-font-size:24px;--awb-margin-bottom:10px;\"><p style=\"font-weight: 300; text-align: left;\"><a href=\"\/de\/diagnostik\/allgemeine-informationen\/probenversand\/\" target=\"_blank\" rel=\"noopener noreferrer\">Hier finden Sie den gesamten Diagnostikablauf<\/a><\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-13 fusion_builder_column_1_1 1_1 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-13 fusion_builder_column_inner_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-padding-top:40px;--awb-padding-right:20px;--awb-padding-bottom:40px;--awb-padding-left:20px;--awb-overflow:hidden;--awb-bg-color:var(--awb-color5);--awb-bg-color-hover:var(--awb-color5);--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-margin-bottom-medium:20px;--awb-spacing-left-medium:7.68%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element fusion-no-small-visibility\" style=\"text-align:center;--awb-max-width:15%;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-7 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"80\" height=\"80\" alt=\"Icon Prozessablauf\" title=\"cegat_icon_prozessablauf\" src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1.png\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1-80x80.png\" class=\"lazyload img-responsive wp-image-5364\" srcset=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27300%27%20viewBox%3D%270%200%20300%20300%27%3E%3Crect%20width%3D%27300%27%20height%3D%27300%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-srcset=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1-200x200.png 200w, https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1.png 300w\" data-sizes=\"auto\" data-orig-sizes=\"(max-width: 768px) 100vw, 80px\" \/><\/span><\/div><div class=\"fusion-separator fusion-no-small-visibility fusion-no-medium-visibility fusion-full-width-sep\" style=\"align-self: center;margin-left: auto;margin-right: auto;margin-bottom:10px;width:100%;\"><\/div><div class=\"fusion-title title fusion-title-22 fusion-sep-none fusion-title-center fusion-title-text fusion-title-size-four\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-bottom:25px;--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h4 class=\"fusion-title-heading title-heading-center fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:24;--minFontSize:24;line-height:1.2;\">Beratung &amp; Auswahl des Tests<\/h4><\/div><div class=\"fusion-separator fusion-no-small-visibility fusion-no-medium-visibility fusion-full-width-sep\" style=\"align-self: center;margin-left: auto;margin-right: auto;margin-bottom:20px;width:100%;\"><\/div><div class=\"fusion-image-element fusion-no-medium-visibility fusion-no-large-visibility\" style=\"text-align:center;--awb-max-width:10%;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-8 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"80\" height=\"80\" alt=\"Icon zur Darstellung eines Prozessablaufs\" title=\"cegat_icon_prozessablauf_mobile\" src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf_mobile-e1674635669710.png\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf_mobile-e1674635669710-80x80.png\" class=\"lazyload img-responsive wp-image-5367\" srcset=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27300%27%20viewBox%3D%270%200%20300%20300%27%3E%3Crect%20width%3D%27300%27%20height%3D%27300%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-srcset=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf_mobile-e1674635669710-200x200.png 200w, https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf_mobile-e1674635669710.png 300w\" data-sizes=\"auto\" data-orig-sizes=\"(max-width: 768px) 100vw, 80px\" \/><\/span><\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-14 fusion_builder_column_inner_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-padding-top:40px;--awb-padding-right:20px;--awb-padding-bottom:40px;--awb-padding-left:20px;--awb-overflow:hidden;--awb-bg-color:var(--awb-color5);--awb-bg-color-hover:var(--awb-color5);--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-margin-bottom-medium:20px;--awb-spacing-left-medium:7.68%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element fusion-no-small-visibility\" style=\"text-align:center;--awb-max-width:15%;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-9 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"80\" height=\"80\" alt=\"Icon Prozessablauf\" title=\"cegat_icon_prozessablauf\" src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1.png\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1-80x80.png\" class=\"lazyload img-responsive wp-image-5364\" srcset=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27300%27%20viewBox%3D%270%200%20300%20300%27%3E%3Crect%20width%3D%27300%27%20height%3D%27300%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-srcset=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1-200x200.png 200w, https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1.png 300w\" data-sizes=\"auto\" data-orig-sizes=\"(max-width: 768px) 100vw, 80px\" \/><\/span><\/div><div class=\"fusion-separator fusion-no-small-visibility fusion-no-medium-visibility fusion-full-width-sep\" style=\"align-self: center;margin-left: auto;margin-right: auto;margin-bottom:10px;width:100%;\"><\/div><div class=\"fusion-title title fusion-title-23 fusion-sep-none fusion-title-center fusion-title-text fusion-title-size-four\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h4 class=\"fusion-title-heading title-heading-center fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:24;--minFontSize:24;line-height:1.2;\">Probenentnahme &amp; Probenversand<\/h4><\/div><div class=\"fusion-image-element fusion-no-medium-visibility fusion-no-large-visibility\" style=\"text-align:center;--awb-max-width:10%;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-10 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"80\" height=\"80\" alt=\"Icon zur Darstellung eines Prozessablaufs\" title=\"cegat_icon_prozessablauf_mobile\" src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf_mobile-e1674635669710.png\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf_mobile-e1674635669710-80x80.png\" class=\"lazyload img-responsive wp-image-5367\" srcset=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27300%27%20viewBox%3D%270%200%20300%20300%27%3E%3Crect%20width%3D%27300%27%20height%3D%27300%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-srcset=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf_mobile-e1674635669710-200x200.png 200w, https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf_mobile-e1674635669710.png 300w\" data-sizes=\"auto\" data-orig-sizes=\"(max-width: 768px) 100vw, 80px\" \/><\/span><\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-15 fusion_builder_column_inner_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-padding-top:40px;--awb-padding-right:20px;--awb-padding-bottom:40px;--awb-padding-left:20px;--awb-overflow:hidden;--awb-bg-color:var(--awb-color5);--awb-bg-color-hover:var(--awb-color5);--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-margin-bottom-small:20px;--awb-spacing-left-small:1.92%;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element fusion-no-small-visibility\" style=\"text-align:center;--awb-max-width:15%;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-11 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"80\" height=\"80\" alt=\"Icon Prozessablauf\" title=\"cegat_icon_prozessablauf\" src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1.png\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1-80x80.png\" class=\"lazyload img-responsive wp-image-5364\" srcset=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27300%27%20viewBox%3D%270%200%20300%20300%27%3E%3Crect%20width%3D%27300%27%20height%3D%27300%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-srcset=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1-200x200.png 200w, https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1.png 300w\" data-sizes=\"auto\" data-orig-sizes=\"(max-width: 768px) 100vw, 80px\" \/><\/span><\/div><div class=\"fusion-separator fusion-no-small-visibility fusion-no-medium-visibility fusion-full-width-sep\" style=\"align-self: center;margin-left: auto;margin-right: auto;margin-bottom:10px;width:100%;\"><\/div><div class=\"fusion-title title fusion-title-24 fusion-sep-none fusion-title-center fusion-title-text fusion-title-size-four\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h4 class=\"fusion-title-heading title-heading-center fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:24;--minFontSize:24;line-height:1.2;\">Analyse der Probe<\/h4><\/div><div class=\"fusion-image-element fusion-no-medium-visibility fusion-no-large-visibility\" style=\"text-align:center;--awb-max-width:10%;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-12 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"80\" height=\"80\" alt=\"Icon zur Darstellung eines Prozessablaufs\" title=\"cegat_icon_prozessablauf_mobile\" src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf_mobile-e1674635669710.png\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf_mobile-e1674635669710-80x80.png\" class=\"lazyload img-responsive wp-image-5367\" srcset=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27300%27%20viewBox%3D%270%200%20300%20300%27%3E%3Crect%20width%3D%27300%27%20height%3D%27300%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-srcset=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf_mobile-e1674635669710-200x200.png 200w, https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf_mobile-e1674635669710.png 300w\" data-sizes=\"auto\" data-orig-sizes=\"(max-width: 768px) 100vw, 80px\" \/><\/span><\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-16 fusion_builder_column_inner_1_4 1_4 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-padding-top:40px;--awb-padding-right:20px;--awb-padding-bottom:40px;--awb-padding-left:20px;--awb-padding-bottom-small:85px;--awb-overflow:hidden;--awb-bg-color:var(--awb-color5);--awb-bg-color-hover:var(--awb-color5);--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 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srcset=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27300%27%20viewBox%3D%270%200%20300%20300%27%3E%3Crect%20width%3D%27300%27%20height%3D%27300%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-srcset=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1-200x200.png 200w, https:\/\/cegat.com\/wp-content\/uploads\/2023\/01\/cegat_icon_prozessablauf-1.png 300w\" data-sizes=\"auto\" data-orig-sizes=\"(max-width: 768px) 100vw, 80px\" \/><\/span><\/div><div class=\"fusion-separator fusion-no-small-visibility fusion-no-medium-visibility fusion-full-width-sep\" style=\"align-self: center;margin-left: auto;margin-right: auto;margin-bottom:10px;width:100%;\"><\/div><div class=\"fusion-title title fusion-title-25 fusion-sep-none fusion-title-center fusion-title-text fusion-title-size-four\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h4 class=\"fusion-title-heading title-heading-center fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:24;--minFontSize:24;line-height:1.2;\">Befund\u00fcbermittlung &amp; Beratung<\/h4><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>\n<div id=\"tabelle\" class=\"fusion-container-anchor\"><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-9 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-padding-top:60px;--awb-padding-bottom:60px;--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-stretch fusion-flex-content-wrap\" style=\"max-width:1248px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-14 fusion_builder_column_1_1 1_1 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-26 fusion-sep-none fusion-title-text fusion-title-size-two\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h2 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:36;line-height:var(--awb-typography1-line-height);\">Genverzeichnis<\/h2><\/div>\n    <div class=\"wpdt-c \">\n    \n<input type=\"hidden\" id=\"wdtNonceFrontendEdit\" name=\"wdtNonceFrontendEdit\" value=\"5681cb9395\" \/><input type=\"hidden\" name=\"_wp_http_referer\" value=\"\/de\/wp-json\/wp\/v2\/pages\/16019\" \/>    <input type=\"hidden\" id=\"table_1_desc\" value='{\"tableId\":\"table_1\",\"tableType\":\"xls\",\"selector\":\"#table_1\",\"responsive\":true,\"responsiveAction\":\"cell\",\"infoBlock\":true,\"pagination\":1,\"paginationAlign\":\"right\",\"paginationLayout\":\"full_numbers\",\"paginationLayoutMobile\":\"simple\",\"file_location\":\"wp_media_lib\",\"table_wcag\":0,\"simple_template_id\":0,\"scrollable\":false,\"globalSearch\":true,\"showRowsPerPage\":false,\"hideBeforeLoad\":false,\"pagination_top\":0,\"number_format\":1,\"decimalPlaces\":2,\"spinnerSrc\":\"https:\\\/\\\/cegat.com\\\/wp-content\\\/plugins\\\/wpdatatables\\\/assets\\\/\\\/img\\\/spinner.gif\",\"groupingEnabled\":false,\"tableWpId\":42,\"dataTableParams\":{\"sDom\":\"BT\\u003C\\u0027clear\\u0027\\u003Eftip\",\"bSortCellsTop\":false,\"bPaginate\":true,\"sPaginationType\":\"full_numbers\",\"aLengthMenu\":[[1,5,10,25,50,100,-1],[1,5,10,25,50,100,\"Alle\"]],\"iDisplayLength\":25,\"columnDefs\":[{\"sType\":\"string\",\"wdtType\":\"string\",\"bVisible\":true,\"orderable\":true,\"searchable\":true,\"InputType\":\"text\",\"name\":\"Gen\",\"origHeader\":\"Gen\",\"notNull\":false,\"conditionalFormattingRules\":[],\"className\":\" 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column-stufe-2\",\"aTargets\":[3]},{\"sType\":\"string\",\"wdtType\":\"string\",\"bVisible\":true,\"orderable\":true,\"searchable\":true,\"InputType\":\"text\",\"name\":\"Stufe 3\",\"origHeader\":\"Stufe 3\",\"notNull\":false,\"conditionalFormattingRules\":[],\"className\":\" column-stufe-3\",\"aTargets\":[4]},{\"sType\":\"formatted-num\",\"wdtType\":\"float\",\"bVisible\":true,\"orderable\":true,\"searchable\":true,\"InputType\":\"text\",\"name\":\"Kilobasen\",\"origHeader\":\"Kilobasen\",\"notNull\":false,\"conditionalFormattingRules\":[],\"className\":\"numdata float  column-kilobasen\",\"aTargets\":[5]}],\"bAutoWidth\":false,\"order\":[[0,\"asc\"]],\"ordering\":false,\"buttons\":[],\"oSearch\":{\"bSmart\":false,\"bRegex\":false,\"sSearch\":\"\"}},\"currentSkin\":\"light\",\"tabletWidth\":\"1024\",\"mobileWidth\":\"480\",\"columnsFixed\":0,\"timeFormat\":\"h:i A\",\"datepickFormat\":\"dd\\\/mm\\\/yy\"}'\/>\n\n    <table id=\"table_1\"\n           class=\"           responsive           display nowrap data-t wpDataTable wpDataTableID-42\"\n           style=\"\"\n           data-described-by='table_1_desc'\n           data-wpdatatable_id=\"42\">\n        \n        <!-- Table header -->\n        \n<thead>\n<tr>\n                    <th\n        data-class=\"expand\"                class=\" wdtheader sort \"\n        style=\"\">Gen<\/th>        <th\n                        class=\" wdtheader sort \"\n        style=\"\">Krankheit<\/th>        <th\n                        class=\" wdtheader sort \"\n        style=\"\">Stufe 1<\/th>        <th\n                        class=\" wdtheader sort \"\n        style=\"\">Stufe 2<\/th>        <th\n                        class=\" wdtheader sort \"\n        style=\"\">Stufe 3<\/th>        <th\n                        class=\" wdtheader sort numdata float \"\n        style=\"\">Kilobasen<\/th>    <\/tr>\n<\/thead>\n        <!-- \/Table header -->\n\n        <!-- Table body -->\n        \n<tbody>\n        <tr id=\"table_42_row_0\">\n                    <td style=\"\">15q11-13<\/td>\n                    <td style=\"\">Prader-Willi Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">26.700.000,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1\">\n                    <td style=\"\">15q11-13<\/td>\n                    <td style=\"\">Angelman Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">26.700.000,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_2\">\n                    <td style=\"\">AAAS<\/td>\n                    <td style=\"\">Achalsie-, Addison-, Alakrimie-Syndrom, Triple-A-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.641,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_3\">\n                    <td style=\"\">ABCA3<\/td>\n                    <td style=\"\">Interstitielle Lungenerkrankung durch ABCA3-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.115,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_4\">\n                    <td style=\"\">ABCA3<\/td>\n                    <td style=\"\">Kongenitale Alveolarproteinose oder interstitielle Lungenerkrankung (ABCA3-Defizienz)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.115,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_5\">\n                    <td style=\"\">ABCA4<\/td>\n                    <td style=\"\">Zapfen-St\u00e4bchen-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.822,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_6\">\n                    <td style=\"\">ABCA4<\/td>\n                    <td style=\"\">autosomal rezessive Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.822,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_7\">\n                    <td style=\"\">ABCA4<\/td>\n                    <td style=\"\">Altersabh\u00e4ngige Makuladegeneration<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.822,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_8\">\n                    <td style=\"\">ABCA4<\/td>\n                    <td style=\"\">Stargardt Krankheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.822,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_9\">\n                    <td style=\"\">ABCB4<\/td>\n                    <td style=\"\">Gallenblasenerkrankung 1, Cholelithiasis mit niedrigen Phospholipid-Spiegeln<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.861,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_10\">\n                    <td style=\"\">ABCB4<\/td>\n                    <td style=\"\">Progressiv famili\u00e4re und intrahepatische Cholestase 3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.861,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_11\">\n                    <td style=\"\">ABCB4<\/td>\n                    <td style=\"\">Intrahepatische Cholestase 3, in der Schwangerschaft<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.861,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_12\">\n                    <td style=\"\">ABCD1<\/td>\n                    <td style=\"\">Adrenoleukodystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.238,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_13\">\n                    <td style=\"\">ABHD12<\/td>\n                    <td style=\"\">Polyneuropathie, Taubheit, Ataxie, Retinitis pigmentosa und Katarakt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.215,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_14\">\n                    <td style=\"\">ABHD5<\/td>\n                    <td style=\"\">Dorfman-Chanarin-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.050,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_15\">\n                    <td style=\"\">ACADS<\/td>\n                    <td style=\"\">Acyl-CoA-Dehydrogenase (SCAD)-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.239,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_16\">\n                    <td style=\"\">ACTA1<\/td>\n                    <td style=\"\">Nemalin-Myopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.134,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_17\">\n                    <td style=\"\">ACTA1<\/td>\n                    <td style=\"\">kongenitale Myopathie mit Fasertyp-Disproportion<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.134,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_18\">\n                    <td style=\"\">ACTA2<\/td>\n                    <td style=\"\">MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.176,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_19\">\n                    <td style=\"\">ACTA2<\/td>\n                    <td style=\"\">AORTIC ANEURYSM, FAMILIAL THORACIC 6; AAT6<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.176,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_20\">\n                    <td style=\"\">ACTA2<\/td>\n                    <td style=\"\">MOYAMOYA DISEASE 5; MYMY5<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.176,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_21\">\n                    <td style=\"\">ACTG2<\/td>\n                    <td style=\"\">Viszerale Myopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.131,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_22\">\n                    <td style=\"\">ACVRL1<\/td>\n                    <td style=\"\">Heredit\u00e4re h\u00e4morrhagische Teleangiektasie, Typ 2; Morbus Osler, Rendu-Osler-Weber-Krankheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.554,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_23\">\n                    <td style=\"\">ADA2<\/td>\n                    <td style=\"\">Polyarteritis nodosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.536,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_24\">\n                    <td style=\"\">ADAR<\/td>\n                    <td style=\"\">Symmetrische und heredit\u00e4re Dyschromie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.711,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_25\">\n                    <td style=\"\">ADAR<\/td>\n                    <td style=\"\">Aicardi-Gouti\u00e8res-Syndrom 6<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.711,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_26\">\n                    <td style=\"\">ADCY5<\/td>\n                    <td style=\"\">Famili\u00e4re Dyskinesie mit Myokymie im Gesicht<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.861,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_27\">\n                    <td style=\"\">ADSL<\/td>\n                    <td style=\"\">Adenylosuccinat Lyase Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.581,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_28\">\n                    <td style=\"\">AGA<\/td>\n                    <td style=\"\">Aspartylglukosaminurie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_29\">\n                    <td style=\"\">AGL<\/td>\n                    <td style=\"\">Glykogen-Speicherkrankheit Typ 3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.599,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_30\">\n                    <td style=\"\">AGPS<\/td>\n                    <td style=\"\">Chondrodysplasia punctata, rhizomeler Typ<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.031,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_31\">\n                    <td style=\"\">AGXT<\/td>\n                    <td style=\"\">Prim\u00e4re Hyperoxalurie Typ 1<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.179,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_32\">\n                    <td style=\"\">AHI1<\/td>\n                    <td style=\"\">Joubert Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.591,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_33\">\n                    <td style=\"\">AICDA<\/td>\n                    <td style=\"\">Hyper-IgM-Syndrom Typ 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">630,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_34\">\n                    <td style=\"\">AIPL1<\/td>\n                    <td style=\"\">Zapfen-St\u00e4bchen-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.155,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_35\">\n                    <td style=\"\">AIPL1<\/td>\n                    <td style=\"\">Juvenile Retinits Pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.155,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_36\">\n                    <td style=\"\">AIPL1<\/td>\n                    <td style=\"\">Leber Congenitale Amaurose 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.155,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_37\">\n                    <td style=\"\">AKT3<\/td>\n                    <td style=\"\">Hemimegalenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.440,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_38\">\n                    <td style=\"\">AKT3<\/td>\n                    <td style=\"\">Hemimegalenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.440,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_39\">\n                    <td style=\"\">ALDH4A1<\/td>\n                    <td style=\"\">Hyperprolin\u00e4mie Typ II<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.692,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_40\">\n                    <td style=\"\">ALDH5A1<\/td>\n                    <td style=\"\">Succinat-Semi-Aldehyd-Dehydrogenase-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.647,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_41\">\n                    <td style=\"\">ALDH7A1<\/td>\n                    <td style=\"\">Pyridoxin-abh\u00e4ngige Epilepsie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.620,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_42\">\n                    <td style=\"\">ALDOB<\/td>\n                    <td style=\"\">Fruktoseintoleranz, heredit\u00e4re<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.095,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_43\">\n                    <td style=\"\">ALG12<\/td>\n                    <td style=\"\">CDG-Syndrom 1G<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.467,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_44\">\n                    <td style=\"\">ALG2<\/td>\n                    <td style=\"\">CDG-Syndrom 1I<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.251,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_45\">\n                    <td style=\"\">ALG3<\/td>\n                    <td style=\"\">CDG-Syndrom 1D<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.317,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_46\">\n                    <td style=\"\">ALG6<\/td>\n                    <td style=\"\">CDG-Syndrome 1C<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.524,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_47\">\n                    <td style=\"\">ALG8<\/td>\n                    <td style=\"\">CDG Syndrom 1H<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.683,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_48\">\n                    <td style=\"\">ALG9<\/td>\n                    <td style=\"\">CDG-Syndrom 1L<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.857,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_49\">\n                    <td style=\"\">ALMS1<\/td>\n                    <td style=\"\">Alstr\u00f6m-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">12.504,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_50\">\n                    <td style=\"\">ALPL<\/td>\n                    <td style=\"\">Hypophosphatasie, infantile<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.575,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_51\">\n                    <td style=\"\">ALPL<\/td>\n                    <td style=\"\">Hypophosphatasie des Erwachsenen<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.575,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_52\">\n                    <td style=\"\">ALPL<\/td>\n                    <td style=\"\">Hypophosphatasie mit Beginn im Kindesalter<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.575,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_53\">\n                    <td style=\"\">ALPL<\/td>\n                    <td style=\"\">Odontohypophosphatasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.575,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_54\">\n                    <td style=\"\">ALS2<\/td>\n                    <td style=\"\">Amyotrophe Lateralsklerose (ALS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.076,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_55\">\n                    <td style=\"\">AMACR<\/td>\n                    <td style=\"\">Gallens\u00e4uresynthesedefekt, kongenitaler, Typ 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.185,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_56\">\n                    <td style=\"\">AMPD1<\/td>\n                    <td style=\"\">Adenosinmonophosphat-Desaminase-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.244,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_57\">\n                    <td style=\"\">AMT<\/td>\n                    <td style=\"\">Nicht-ketotische Hyperglyzin\u00e4mie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.212,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_58\">\n                    <td style=\"\">ANG<\/td>\n                    <td style=\"\">Amyotrophe Lateralsklerose (ALS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">444,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_59\">\n                    <td style=\"\">ANO10<\/td>\n                    <td style=\"\">Spinocerebell\u00e4re Ataxie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.983,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_60\">\n                    <td style=\"\">ANO3<\/td>\n                    <td style=\"\">Dystonie, DYT24, Kraniozervikale Dystonie mit Beteiligung des Larynx und der oberen Extremit\u00e4ten<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.129,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_61\">\n                    <td style=\"\">AP2S1<\/td>\n                    <td style=\"\">Famili\u00e4re, hypokalzurische Hyperkalz\u00e4mie Typ III<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">477,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_62\">\n                    <td style=\"\">APOA1<\/td>\n                    <td style=\"\">Apolipoprotein A-I-Amyloidose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">804,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_63\">\n                    <td style=\"\">APOA1<\/td>\n                    <td style=\"\">Amyloidose Apolipoprotein A-I-Mangel Hypoalphalipoprotein\u00e4mie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">804,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_64\">\n                    <td style=\"\">APOA1<\/td>\n                    <td style=\"\">Apolipoprotein A 1-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">804,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_65\">\n                    <td style=\"\">APOA2<\/td>\n                    <td style=\"\">Apolipoprotein A-II-Defizienz, AApoAII-Amyloidose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">303,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_66\">\n                    <td style=\"\">APOA5<\/td>\n                    <td style=\"\">Hyperlipoprotein\u00e4mie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.185,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_67\">\n                    <td style=\"\">APP<\/td>\n                    <td style=\"\">Alzheimer Demenz<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.313,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_68\">\n                    <td style=\"\">APTX<\/td>\n                    <td style=\"\">Ataxie - okulomotorische Apraxie, Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.029,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_69\">\n                    <td style=\"\">AQP2<\/td>\n                    <td style=\"\">Nephrogener Diabetes insipidus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">816,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_70\">\n                    <td style=\"\">AR<\/td>\n                    <td style=\"\">Androgenresistenz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Fragmentl\u00e4ngenanalyse<\/td>\n                    <td style=\"\">2.763,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_71\">\n                    <td style=\"\">AR<\/td>\n                    <td style=\"\">Muskelatrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Fragmentl\u00e4ngenanalyse<\/td>\n                    <td style=\"\">2.763,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_72\">\n                    <td style=\"\">AR<\/td>\n                    <td style=\"\">Kennedy-Syndrom (Spinale and Bulb\u00e4re Muskelatrophie, X-gekoppelt 1; SMAX1)<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.763,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_73\">\n                    <td style=\"\">ARFGEF2<\/td>\n                    <td style=\"\">Periventrikul\u00e4re nodul\u00e4re Heterotopie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.358,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_74\">\n                    <td style=\"\">ARHGEF9<\/td>\n                    <td style=\"\">heredit\u00e4re Hyperekplexie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.590,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_75\">\n                    <td style=\"\">ARSA<\/td>\n                    <td style=\"\">Metachromatische Leukodystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.530,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_76\">\n                    <td style=\"\">ARSB<\/td>\n                    <td style=\"\">Mukopolysaccharidose Typ VI-A (Morbus Maroteaux-Lamy)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.602,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_77\">\n                    <td style=\"\">ARSI<\/td>\n                    <td style=\"\">Spastic Paraplegia Type 66<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.710,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_78\">\n                    <td style=\"\">ARX<\/td>\n                    <td style=\"\">Mikrozephalie - Corpus callosum-Agenesie - Genitalfehlbildung<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.689,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_79\">\n                    <td style=\"\">ARX<\/td>\n                    <td style=\"\">West-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.689,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_80\">\n                    <td style=\"\">ARX<\/td>\n                    <td style=\"\">X-chromosomale Lissenzephalie mit Genitalanomalien<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.689,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_81\">\n                    <td style=\"\">ARX<\/td>\n                    <td style=\"\">X-chromosomale Lissenzephalie mit Genitalanomalien<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.689,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_82\">\n                    <td style=\"\">ARX<\/td>\n                    <td style=\"\">West-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.689,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_83\">\n                    <td style=\"\">ARX<\/td>\n                    <td style=\"\">Partington-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.689,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_84\">\n                    <td style=\"\">ASAH1<\/td>\n                    <td style=\"\">Progressive distale Muskelatrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.236,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_85\">\n                    <td style=\"\">ASAH1<\/td>\n                    <td style=\"\">Farber-Lipogranulomatose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.236,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_86\">\n                    <td style=\"\">ASPM<\/td>\n                    <td style=\"\">Isolierte kongenitale Mikrozephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">10.656,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_87\">\n                    <td style=\"\">ASXL1<\/td>\n                    <td style=\"\">Bohring-Opitz Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.626,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_88\">\n                    <td style=\"\">ATF6<\/td>\n                    <td style=\"\">Achromatopsie 7<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.103,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_89\">\n                    <td style=\"\">ATL1<\/td>\n                    <td style=\"\">Heredit\u00e4re sensorische und autonome Neuropathie Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.860,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_90\">\n                    <td style=\"\">ATL1<\/td>\n                    <td style=\"\">Spastische Paraplegie Typ 3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.860,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_91\">\n                    <td style=\"\">ATM<\/td>\n                    <td style=\"\">Ataxia teleangiectatica (AT)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">9.171,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_92\">\n                    <td style=\"\">ATP13A2<\/td>\n                    <td style=\"\">Kufor-Rakeb Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.543,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_93\">\n                    <td style=\"\">ATP1A2<\/td>\n                    <td style=\"\">Famili\u00e4re hemiplegische Migr\u00e4ne Typ 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.063,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_94\">\n                    <td style=\"\">ATP1A3<\/td>\n                    <td style=\"\">Rapid Onset Dystonie mit Parkinsonismus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.081,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_95\">\n                    <td style=\"\">ATP2A1<\/td>\n                    <td style=\"\">Brody Myopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.006,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_96\">\n                    <td style=\"\">ATP2A2<\/td>\n                    <td style=\"\">Darier-Krankheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.129,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_97\">\n                    <td style=\"\">ATP2C1<\/td>\n                    <td style=\"\">Morbus Hailey-Hailey, Pemphigus, benigner chronischer famili\u00e4rer<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.922,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_98\">\n                    <td style=\"\">ATP6AP2<\/td>\n                    <td style=\"\">Geistige Retardierung - Epilepsie, X-chromosomaler rezessiver Typ<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.053,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_99\">\n                    <td style=\"\">ATP6V0A4<\/td>\n                    <td style=\"\">Azidose, renale tubul\u00e4re, distale, autosomal-rezessive Form<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.523,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_100\">\n                    <td style=\"\">ATP6V1B1<\/td>\n                    <td style=\"\">Renale tubul\u00e4re Azidose mit Taubheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.542,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_101\">\n                    <td style=\"\">ATP7A<\/td>\n                    <td style=\"\">ATP7A-assoziierte Erkrankungen<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.596,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_102\">\n                    <td style=\"\">ATP7A<\/td>\n                    <td style=\"\">Menkes-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.596,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_103\">\n                    <td style=\"\">ATP7B<\/td>\n                    <td style=\"\">Morbus Wilson<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.398,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_104\">\n                    <td style=\"\">ATP8A2<\/td>\n                    <td style=\"\">Zerebell\u00e4re Ataxie, Mentale Retardierung und Dis\u00e4quilibrium Syndrom 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.567,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_105\">\n                    <td style=\"\">ATP8B1<\/td>\n                    <td style=\"\">Cholestase, intrahepatische progressive, famili\u00e4re, Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.756,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_106\">\n                    <td style=\"\">ATP8B1<\/td>\n                    <td style=\"\">Gutartige, wiederkehrende und intrahepatische Cholestase Typ1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.756,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_107\">\n                    <td style=\"\">ATP8B1<\/td>\n                    <td style=\"\">Intrahepatische Cholestase 1, in der Schwangerschaft<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.756,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_108\">\n                    <td style=\"\">ATRX<\/td>\n                    <td style=\"\">X-chromosomale Alpha-Thalass\u00e4mie-Geistige Retardierung-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">7.479,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_109\">\n                    <td style=\"\">ATXN1<\/td>\n                    <td style=\"\">Ataxie, spinozerebell\u00e4re, Typ 1<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.448,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_110\">\n                    <td style=\"\">ATXN2<\/td>\n                    <td style=\"\">Ataxie, spinozerebell\u00e4re, Typ 2<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.942,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_111\">\n                    <td style=\"\">ATXN3<\/td>\n                    <td style=\"\">Machado-Joseph Krankheit<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.095,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_112\">\n                    <td style=\"\">ATXN7<\/td>\n                    <td style=\"\">Ataxie, spinozerebell\u00e4re, Typ 7<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.838,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_113\">\n                    <td style=\"\">B9D1<\/td>\n                    <td style=\"\">Meckel Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">615,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_114\">\n                    <td style=\"\">B9D2<\/td>\n                    <td style=\"\">Meckel Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">528,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_115\">\n                    <td style=\"\">BBS1<\/td>\n                    <td style=\"\">Bardet-Biedl-Syndrom (BBS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.782,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_116\">\n                    <td style=\"\">BBS2<\/td>\n                    <td style=\"\">Bardet Biedl Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.211,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_117\">\n                    <td style=\"\">BCKDHA<\/td>\n                    <td style=\"\">Ahornsirupkrankheit Typ 1A<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.338,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_118\">\n                    <td style=\"\">BCKDHB<\/td>\n                    <td style=\"\">Ahornsirupkrankheit\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.179,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_119\">\n                    <td style=\"\">BEST1<\/td>\n                    <td style=\"\">autosomal dominante Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.815,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_120\">\n                    <td style=\"\">BEST1<\/td>\n                    <td style=\"\">autosomal rezessive Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.815,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_121\">\n                    <td style=\"\">BFSP2<\/td>\n                    <td style=\"\">heredit\u00e4re Katarakt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.248,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_122\">\n                    <td style=\"\">BICD2<\/td>\n                    <td style=\"\">Spinale Muskelatrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.568,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_123\">\n                    <td style=\"\">BSCL2<\/td>\n                    <td style=\"\">Lipodystrophie Typ Berardinelli<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.398,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_124\">\n                    <td style=\"\">BSCL2<\/td>\n                    <td style=\"\">Spastische Paraplegie, Typ 17<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.398,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_125\">\n                    <td style=\"\">BSCL2<\/td>\n                    <td style=\"\">distale heredit\u00e4re motorische Neuropathie, Typ 5<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.398,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_126\">\n                    <td style=\"\">BTD<\/td>\n                    <td style=\"\">Biotinidase-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.572,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_127\">\n                    <td style=\"\">C1QA<\/td>\n                    <td style=\"\">C1q DEFICIENCY; C1QD<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">738,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_128\">\n                    <td style=\"\">C1QC<\/td>\n                    <td style=\"\">C1q DEFICIENCY; C1QD<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">738,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_129\">\n                    <td style=\"\">C1QTNF5<\/td>\n                    <td style=\"\">Sp\u00e4t beginnende Netzhautdystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">732,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_130\">\n                    <td style=\"\">C9orf72<\/td>\n                    <td style=\"\">Amyotrophe Lateralsklerose (ALS)<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.479,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_131\">\n                    <td style=\"\">CABP4<\/td>\n                    <td style=\"\">Kongenitale station\u00e4re Nachtblindheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">828,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_132\">\n                    <td style=\"\">CACNA1A<\/td>\n                    <td style=\"\">Famili\u00e4re hemiplegische Migr\u00e4ne Typ 1\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\">7.539,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_133\">\n                    <td style=\"\">CACNA1A<\/td>\n                    <td style=\"\">Spinocerebell\u00e4re Ataxie Typ 6<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\">7.539,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_134\">\n                    <td style=\"\">CACNA1A<\/td>\n                    <td style=\"\">Paroxysmale famili\u00e4re Ataxie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\">7.539,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_135\">\n                    <td style=\"\">CACNA1A<\/td>\n                    <td style=\"\">Episodische Ataxie - Typ 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\">7.539,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_136\">\n                    <td style=\"\">CACNA1B<\/td>\n                    <td style=\"\">Dystonie, DYT23<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">7.146,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_137\">\n                    <td style=\"\">CACNA1F<\/td>\n                    <td style=\"\">Zapfen-St\u00e4bchen-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.934,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_138\">\n                    <td style=\"\">CACNA1F<\/td>\n                    <td style=\"\">Kongenitale station\u00e4re Nachtblindheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.934,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_139\">\n                    <td style=\"\">CACNA1H<\/td>\n                    <td style=\"\">Absencenepilepsie der Kindheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">7.077,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_140\">\n                    <td style=\"\">CACNA1H<\/td>\n                    <td style=\"\">famili\u00e4rer Hyperaldosteronismus Typ  IV, Absencen-Epilepsie des Kindesalters<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">7.077,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_141\">\n                    <td style=\"\">CACNB4<\/td>\n                    <td style=\"\">Idiopathische generalisierte Epilepsie (IGE)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.563,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_142\">\n                    <td style=\"\">CACNB4<\/td>\n                    <td style=\"\">Episodische Ataxie - Typ 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.563,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_143\">\n                    <td style=\"\">CACNB4<\/td>\n                    <td style=\"\">Juvenile Myoklonus Epilepsie (JME)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.563,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_144\">\n                    <td style=\"\">CAPN3<\/td>\n                    <td style=\"\">Autosomal-rezessive Gliederg\u00fcrtelmuskeldystrophie, Typ 2A<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.466,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_145\">\n                    <td style=\"\">CASK<\/td>\n                    <td style=\"\">FG-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.868,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_146\">\n                    <td style=\"\">CASK<\/td>\n                    <td style=\"\">X-chromosomale geistige Retardierung, Typ Najm<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.868,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_147\">\n                    <td style=\"\">CASR<\/td>\n                    <td style=\"\">Famili\u00e4re hypokalziurische Hyperkalz\u00e4mie (FHH)<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.267,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_148\">\n                    <td style=\"\">CASR<\/td>\n                    <td style=\"\">Schwerer prim\u00e4rer neonataler Hyperparathyreoidismus<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.267,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_149\">\n                    <td style=\"\">CASR<\/td>\n                    <td style=\"\">Autosomal-dominante Hypokalz\u00e4mie (ADH)<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.267,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_150\">\n                    <td style=\"\">CAVIN1<\/td>\n                    <td style=\"\">Lipodystrophy, congenital generalized, type 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.173,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_151\">\n                    <td style=\"\">CCDC65<\/td>\n                    <td style=\"\">Prim\u00e4re zili\u00e4re Dyskinesie, 27<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.455,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_152\">\n                    <td style=\"\">CCN6<\/td>\n                    <td style=\"\">progressive pseudorheumatoide Arthropathie der Kindheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.065,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_153\">\n                    <td style=\"\">CCND2<\/td>\n                    <td style=\"\">Megalenzephalie - Polymikrogyrie - postaxiale Polydaktylie - Hydrozephalus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">912,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_154\">\n                    <td style=\"\">CCNQ<\/td>\n                    <td style=\"\">STAR Syndrom (Syndaktylie - Telekanthus - anogenitale und renale Fehlbildunge)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">741,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_155\">\n                    <td style=\"\">CD96<\/td>\n                    <td style=\"\">C-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.758,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_156\">\n                    <td style=\"\">CDH3<\/td>\n                    <td style=\"\">Hypotrichose mit juveniler Makuladystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.490,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_157\">\n                    <td style=\"\">CDH3<\/td>\n                    <td style=\"\">EEM-Syndrom, Dysplasie, ektodermale - Ektrodaktylie - Makuladystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.490,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_158\">\n                    <td style=\"\">CDHR1<\/td>\n                    <td style=\"\">Zapfen-St\u00e4bchen-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.580,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_159\">\n                    <td style=\"\">CDHR1<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.580,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_160\">\n                    <td style=\"\">CDK5RAP2<\/td>\n                    <td style=\"\">prim\u00e4re autosomal-rezessive Mikrozephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.682,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_161\">\n                    <td style=\"\">CDKL5<\/td>\n                    <td style=\"\">West-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.093,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_162\">\n                    <td style=\"\">CDKL5<\/td>\n                    <td style=\"\">fr\u00fchinfantile epileptische  Enzephalopathie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.093,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_163\">\n                    <td style=\"\">CDKL5<\/td>\n                    <td style=\"\">West-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.093,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_164\">\n                    <td style=\"\">CDKL5<\/td>\n                    <td style=\"\">atypisches Rett-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.093,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_165\">\n                    <td style=\"\">CDON<\/td>\n                    <td style=\"\">Holoprosenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.864,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_166\">\n                    <td style=\"\">CEP63<\/td>\n                    <td style=\"\">Seckel Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.112,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_167\">\n                    <td style=\"\">CFAP410<\/td>\n                    <td style=\"\">Zapfen-St\u00e4bchen-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.128,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_168\">\n                    <td style=\"\">CFAP410<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.128,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_169\">\n                    <td style=\"\">CFAP410<\/td>\n                    <td style=\"\">Spondylometaphyseale Dysplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.128,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_170\">\n                    <td style=\"\">CFAP410<\/td>\n                    <td style=\"\">Jeune Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.128,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_171\">\n                    <td style=\"\">CFAP410<\/td>\n                    <td style=\"\">Retinale Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.128,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_172\">\n                    <td style=\"\">CFH<\/td>\n                    <td style=\"\">H\u00e4molytisch-ur\u00e4misches Syndrom, atypische Form mit H-Faktor-Anomalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.696,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_173\">\n                    <td style=\"\">CFH<\/td>\n                    <td style=\"\">Famili\u00e4re Drusen<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.696,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_174\">\n                    <td style=\"\">CFH<\/td>\n                    <td style=\"\">Altersabh\u00e4ngige Makuladegeneration<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.696,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_175\">\n                    <td style=\"\">CFTR<\/td>\n                    <td style=\"\">Zystische Fibrose<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">4.443,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_176\">\n                    <td style=\"\">CFTR<\/td>\n                    <td style=\"\">Kongenitale, bilaterale-Aplasie des Vas deferens (CBAVD)<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">4.443,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_177\">\n                    <td style=\"\">CHCHD10<\/td>\n                    <td style=\"\">Spinale Muskelatrophy, Jokela Typ<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">450,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_178\">\n                    <td style=\"\">CHCHD10<\/td>\n                    <td style=\"\">Frontotemporale Demenz mit Motoneuron-Krankheit 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">450,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_179\">\n                    <td style=\"\">CHCHD10<\/td>\n                    <td style=\"\">Autosomal-dominante mitochondriale Myopathie mit Belastungsintoleranz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">450,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_180\">\n                    <td style=\"\">CHD2<\/td>\n                    <td style=\"\">Epilepsie mit myoklonisch-astatischen Krisen, Lennox-Gastaut-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.487,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_181\">\n                    <td style=\"\">CHD7<\/td>\n                    <td style=\"\">Hypogonadismus, hypogonadotroper normosmischer, kongenitale Form, 5<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.994,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_182\">\n                    <td style=\"\">CHD7<\/td>\n                    <td style=\"\">Hypogonadotroper Hypogonadismus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.994,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_183\">\n                    <td style=\"\">CHD7<\/td>\n                    <td style=\"\">CHARGE Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.994,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_184\">\n                    <td style=\"\">CHKB<\/td>\n                    <td style=\"\">Kongenitale Muskeldystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.188,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_185\">\n                    <td style=\"\">CHM<\/td>\n                    <td style=\"\">Choroidalsklerose<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.962,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_186\">\n                    <td style=\"\">CHMP2B<\/td>\n                    <td style=\"\">Frontotemporale Demenz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">690,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_187\">\n                    <td style=\"\">CHN1<\/td>\n                    <td style=\"\">Duane-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.380,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_188\">\n                    <td style=\"\">CHRNA1<\/td>\n                    <td style=\"\">Multiples Pterygium-Syndrom, letale Form<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.449,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_189\">\n                    <td style=\"\">CHRNA1<\/td>\n                    <td style=\"\">Myasthenes Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.449,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_190\">\n                    <td style=\"\">CHRNA2<\/td>\n                    <td style=\"\">N\u00e4chtliche Frontallappen- Epilepsie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.590,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_191\">\n                    <td style=\"\">CHRNA4<\/td>\n                    <td style=\"\">N\u00e4chtliche Frontallappen- Epilepsie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.884,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_192\">\n                    <td style=\"\">CHRNB1<\/td>\n                    <td style=\"\">Myasthenische Syndrome<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.506,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_193\">\n                    <td style=\"\">CHRNB2<\/td>\n                    <td style=\"\">N\u00e4chtliche Frontallappen- Epilepsie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.509,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_194\">\n                    <td style=\"\">CHRNB3<\/td>\n                    <td style=\"\">Amyotrophe Lateralsklerose (ALS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.377,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_195\">\n                    <td style=\"\">CHRND<\/td>\n                    <td style=\"\">Myasthenes Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.554,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_196\">\n                    <td style=\"\">CHRND<\/td>\n                    <td style=\"\">Multiples Pterygium-Syndrom, letale Form<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.554,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_197\">\n                    <td style=\"\">CIZ1<\/td>\n                    <td style=\"\">Dystonie, DYT23<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.865,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_198\">\n                    <td style=\"\">CLCN1<\/td>\n                    <td style=\"\">Myotonia congenita Typ Thomsen und Becker<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.967,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_199\">\n                    <td style=\"\">CLCN5<\/td>\n                    <td style=\"\">Proteinuria und hypercalciurische Nephrocalicnose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.451,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_200\">\n                    <td style=\"\">CLCN5<\/td>\n                    <td style=\"\">Hypophosphat\u00e4mische Rachitiden<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.451,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_201\">\n                    <td style=\"\">CLCN5<\/td>\n                    <td style=\"\">Dent-Krankheit Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.451,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_202\">\n                    <td style=\"\">CLCN5<\/td>\n                    <td style=\"\">Nephrolithiasis 1 (Nierensteine)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.451,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_203\">\n                    <td style=\"\">CLN3<\/td>\n                    <td style=\"\">Neuronale Ceroid-Lipofuszinose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.317,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_204\">\n                    <td style=\"\">CLN3<\/td>\n                    <td style=\"\">progressive Epilepsie mit Intelligenzminderung, Finnischer Typ<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.317,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_205\">\n                    <td style=\"\">CLN5<\/td>\n                    <td style=\"\">Neuronale Ceroid-Lipofuszinose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.077,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_206\">\n                    <td style=\"\">CLN6<\/td>\n                    <td style=\"\">Neuronale Ceroid-Lipofuszinose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.032,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_207\">\n                    <td style=\"\">CLN8<\/td>\n                    <td style=\"\">Neuronale Ceroid-Lipofuszinose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">861,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_208\">\n                    <td style=\"\">CLPB<\/td>\n                    <td style=\"\">3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.124,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_209\">\n                    <td style=\"\">CLRN1<\/td>\n                    <td style=\"\">Usher Syndrom Typ 3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">738,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_210\">\n                    <td style=\"\">CNGA3<\/td>\n                    <td style=\"\">Achromatopsie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.085,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_211\">\n                    <td style=\"\">CNGB1<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.756,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_212\">\n                    <td style=\"\">CNGB3<\/td>\n                    <td style=\"\">Achromatopsie<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">2.430,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_213\">\n                    <td style=\"\">CNGB3<\/td>\n                    <td style=\"\">Stargardt Krankheit<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">2.430,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_214\">\n                    <td style=\"\">CNTNAP2<\/td>\n                    <td style=\"\">Pitt-Hopkins-\u00e4hnliches Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.996,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_215\">\n                    <td style=\"\">COASY<\/td>\n                    <td style=\"\">Neurodegeneration mit Eisenablagerungim Gehirn 6 (COASY-Protein-assoziierte Neurodegeneration)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.782,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_216\">\n                    <td style=\"\">COASY<\/td>\n                    <td style=\"\">Neurodegeneration mit Eisenablagerung im Gehirn (NBIA)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.782,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_217\">\n                    <td style=\"\">COG6<\/td>\n                    <td style=\"\">CDG-Syndrom Typ II l<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.974,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_218\">\n                    <td style=\"\">COG7<\/td>\n                    <td style=\"\">CDG-Syndrom Typ II e<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.313,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_219\">\n                    <td style=\"\">COL10A1<\/td>\n                    <td style=\"\">Metaphys\u00e4re Dysplasie Typ Schmid<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.043,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_220\">\n                    <td style=\"\">COL18A1<\/td>\n                    <td style=\"\">Knobloch Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.265,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_221\">\n                    <td style=\"\">COL2A1<\/td>\n                    <td style=\"\">Kniest Dysplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.464,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_222\">\n                    <td style=\"\">COL2A1<\/td>\n                    <td style=\"\">Stickler Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.464,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_223\">\n                    <td style=\"\">COL4A1<\/td>\n                    <td style=\"\">COL4A1-assoziierte zerebrale Mikroangiopathie mit H\u00e4morrhagie (Leukenzepahlopathie, famili\u00e4re vaskul\u00e4re, COL4A1-assoziierte)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.010,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_224\">\n                    <td style=\"\">COL4A1<\/td>\n                    <td style=\"\">Tortuosit\u00e4t der retinalen Arterien<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.010,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_225\">\n                    <td style=\"\">COL4A1<\/td>\n                    <td style=\"\">Porenzephalie 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.010,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_226\">\n                    <td style=\"\">COL4A1<\/td>\n                    <td style=\"\">Heredit\u00e4res Angiopathie-Nephropathie-Aneurysmen-Muskelkrampf-Syndrom (HANAC-Syndrom)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.010,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_227\">\n                    <td style=\"\">COL4A3<\/td>\n                    <td style=\"\">H\u00e4maturie, benigne famili\u00e4re<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.013,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_228\">\n                    <td style=\"\">COL4A3<\/td>\n                    <td style=\"\">Alport-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.013,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_229\">\n                    <td style=\"\">COL6A3<\/td>\n                    <td style=\"\">Bethlem-Myopathie 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">9.534,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_230\">\n                    <td style=\"\">COL6A3<\/td>\n                    <td style=\"\">Dystonie, DYT27, prim\u00e4re<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">9.534,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_231\">\n                    <td style=\"\">COL6A3<\/td>\n                    <td style=\"\">Kongenitale Muskeldystrophie Typ Ullrich<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">9.534,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_232\">\n                    <td style=\"\">COL9A1<\/td>\n                    <td style=\"\">Stickler Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.766,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_233\">\n                    <td style=\"\">COL9A1<\/td>\n                    <td style=\"\">Multiple epiphys\u00e4re Dysplasie\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.766,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_234\">\n                    <td style=\"\">COL9A2<\/td>\n                    <td style=\"\">Multiple epiphys\u00e4re Dysplasie\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.070,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_235\">\n                    <td style=\"\">COL9A3<\/td>\n                    <td style=\"\">Multiple epiphys\u00e4re Dysplasie\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.055,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_236\">\n                    <td style=\"\">COLEC11<\/td>\n                    <td style=\"\">Kranio-fazio-ulnar-renales Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">858,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_237\">\n                    <td style=\"\">COMP<\/td>\n                    <td style=\"\">Multiple epiphys\u00e4re Dysplasie\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.274,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_238\">\n                    <td style=\"\">COMP<\/td>\n                    <td style=\"\">Pseudoachondroplasie\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.274,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_239\">\n                    <td style=\"\">COPA<\/td>\n                    <td style=\"\">Autoimmune interstitielle Lungenerkrankung-Arthritis-Syndrom (COPA-Defekt)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.702,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_240\">\n                    <td style=\"\">COQ8A<\/td>\n                    <td style=\"\">Komplex I Defekt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.944,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_241\">\n                    <td style=\"\">COQ8A<\/td>\n                    <td style=\"\">Komplex I Defekt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.944,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_242\">\n                    <td style=\"\">COQ9<\/td>\n                    <td style=\"\">Komplex I Defekt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">957,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_243\">\n                    <td style=\"\">COX15<\/td>\n                    <td style=\"\">Leigh-Syndrom mit Leukodystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.233,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_244\">\n                    <td style=\"\">COX15<\/td>\n                    <td style=\"\">Cytochrom-C-Oxidase Mangel, infantile fatale Form<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.233,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_245\">\n                    <td style=\"\">CP<\/td>\n                    <td style=\"\">Aceruloplasmin\u00e4mie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.198,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_246\">\n                    <td style=\"\">CPA1<\/td>\n                    <td style=\"\">Heredit\u00e4re Pankreatitis (CPA1-Gen)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.260,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_247\">\n                    <td style=\"\">CPT2<\/td>\n                    <td style=\"\">Carnitin-Palmitoyl-Transferase II-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.977,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_248\">\n                    <td style=\"\">CRB1<\/td>\n                    <td style=\"\">Leber Congenitale Amaurose 8<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.221,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_249\">\n                    <td style=\"\">CRB1<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.221,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_250\">\n                    <td style=\"\">CRPPA<\/td>\n                    <td style=\"\">Kongenitale Muskeldystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.356,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_251\">\n                    <td style=\"\">CRX<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">900,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_252\">\n                    <td style=\"\">CRX<\/td>\n                    <td style=\"\">Leber Congenitale Amaurose 7<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">900,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_253\">\n                    <td style=\"\">CSF1R<\/td>\n                    <td style=\"\">Leukoenzephalopathie mit Spheroiden<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.919,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_254\">\n                    <td style=\"\">CSF2RA<\/td>\n                    <td style=\"\">Kongenitale Alveolarproteinose (Mutation in der GM-CSF-Rezeptor-\u03b1- Kette; CSF2RA-Gen)<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.406,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_255\">\n                    <td style=\"\">CSTB<\/td>\n                    <td style=\"\">Progressive Myoclonus Epilepsie mit Ataxie<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">297,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_256\">\n                    <td style=\"\">CSTB<\/td>\n                    <td style=\"\">Unverricht-Lundborg-Krankheit (ULD)<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">297,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_257\">\n                    <td style=\"\">CTLA4<\/td>\n                    <td style=\"\">Autoimmun-lymphoproliferatives Syndrom durch CTLA4-Haploinsuffizienz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">744,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_258\">\n                    <td style=\"\">CTRC<\/td>\n                    <td style=\"\">Risikofaktor f\u00fcr chronische heredit\u00e4re Pankreatitis<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">807,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_259\">\n                    <td style=\"\">CTSD<\/td>\n                    <td style=\"\">Neuronale Ceroid-Lipofuszinose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.239,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_260\">\n                    <td style=\"\">CTSF<\/td>\n                    <td style=\"\">Neuronale Ceroid-Lipofuszinose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.518,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_261\">\n                    <td style=\"\">CTSF<\/td>\n                    <td style=\"\">progressive Epilepsie mit Intelligenzminderung, Finnischer Typ<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.518,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_262\">\n                    <td style=\"\">CYP19A1<\/td>\n                    <td style=\"\">Aromatase-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.512,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_263\">\n                    <td style=\"\">CYP27A1<\/td>\n                    <td style=\"\">Zerebrotendin\u00f6se Xanthomatose (CTX)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.596,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_264\">\n                    <td style=\"\">DARS1<\/td>\n                    <td style=\"\">Hypomyelinisierung mit Hirnstamm- und R\u00fcckenmarkbeteiligung und Beinspastik<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.506,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_265\">\n                    <td style=\"\">DARS2<\/td>\n                    <td style=\"\">Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.938,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_266\">\n                    <td style=\"\">DBT<\/td>\n                    <td style=\"\">Ahornsirupkrankheit\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.575,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_267\">\n                    <td style=\"\">DCC<\/td>\n                    <td style=\"\">Horizontale Blickl\u00e4hmung mit progredienter Skoliose (HGPPS)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.344,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_268\">\n                    <td style=\"\">DCC<\/td>\n                    <td style=\"\">Spiegelbewegungen, famili\u00e4re kongenitale ,1 (Kontralaterale Synkinesie, isolierte kongenitale)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.344,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_269\">\n                    <td style=\"\">DCTN1<\/td>\n                    <td style=\"\">Perry Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.837,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_270\">\n                    <td style=\"\">DCX<\/td>\n                    <td style=\"\">Lissenzephalie Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.326,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_271\">\n                    <td style=\"\">DES<\/td>\n                    <td style=\"\">Myofibrill\u00e4re Myopathie 1, Desminopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.413,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_272\">\n                    <td style=\"\">DES<\/td>\n                    <td style=\"\">Kardiomyopathie, dilatative famili\u00e4re, 1I<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.413,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_273\">\n                    <td style=\"\">DES<\/td>\n                    <td style=\"\">Gliederg\u00fcrtel-Muskeldystrophien Typ 2R (LGMD2R)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.413,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_274\">\n                    <td style=\"\">DES<\/td>\n                    <td style=\"\">Neurogenes scapulo-peroneales Syndrom Typ Kaeser<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.413,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_275\">\n                    <td style=\"\">DGKE<\/td>\n                    <td style=\"\">Membran-proliferative Glomerulonephritis (MPGN)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.704,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_276\">\n                    <td style=\"\">DHTKD1<\/td>\n                    <td style=\"\">2-Alpha-Aminoadipins\u00e4ure-2-Oxoadipins\u00e4ure Azidurie (Alpha-Aminoadipinazidurie)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.760,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_277\">\n                    <td style=\"\">DLD<\/td>\n                    <td style=\"\">Lipoamid-Dehydrogenase (LAD)-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.530,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_278\">\n                    <td style=\"\">DLD<\/td>\n                    <td style=\"\">Leigh-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.530,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_279\">\n                    <td style=\"\">DLD<\/td>\n                    <td style=\"\">Ahornsirupkrankheit\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.530,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_280\">\n                    <td style=\"\">DMD<\/td>\n                    <td style=\"\">Muskeldystrophie Typ Becker<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">11.058,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_281\">\n                    <td style=\"\">DMD<\/td>\n                    <td style=\"\">Muskeldystrophie Typ Duchenne<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">11.058,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_282\">\n                    <td style=\"\">DMD<\/td>\n                    <td style=\"\">Kardiomyopathie, dilatative  (DCM)<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">11.058,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_283\">\n                    <td style=\"\">DMP1<\/td>\n                    <td style=\"\">Hypophosphat\u00e4mische Rachitis, autosomal rezessiv<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.542,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_284\">\n                    <td style=\"\">DNAAF11<\/td>\n                    <td style=\"\">Prim\u00e4re zili\u00e4re Dyskinesie, 19<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.401,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_285\">\n                    <td style=\"\">DNAAF4<\/td>\n                    <td style=\"\">Prim\u00e4re zili\u00e4re Dyskinesie, 25<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.263,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_286\">\n                    <td style=\"\">DNAAF5<\/td>\n                    <td style=\"\">Prim\u00e4re zili\u00e4re Dyskinesie, 18<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.568,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_287\">\n                    <td style=\"\">DNAI1<\/td>\n                    <td style=\"\">Prim\u00e4re zili\u00e4re Dyskinesie, 1, mit oder ohne situs inversus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.112,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_288\">\n                    <td style=\"\">DNAJC5<\/td>\n                    <td style=\"\">Neuronale Ceroid-Lipofuszinose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">597,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_289\">\n                    <td style=\"\">DOK7<\/td>\n                    <td style=\"\">Myasthenes Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.827,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_290\">\n                    <td style=\"\">DPAGT1<\/td>\n                    <td style=\"\">CDG-Syndrom Typ Ij<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.227,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_291\">\n                    <td style=\"\">DRD2<\/td>\n                    <td style=\"\">Myklonus Dystonie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.332,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_292\">\n                    <td style=\"\">DUOX2<\/td>\n                    <td style=\"\">Schilddr\u00fcsen Dyshormonogenese 6<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.647,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_293\">\n                    <td style=\"\">DUOXA2<\/td>\n                    <td style=\"\">Schilddr\u00fcsen Dyshormonogenese 5<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">963,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_294\">\n                    <td style=\"\">DYSF<\/td>\n                    <td style=\"\">Gliederg\u00fcrtel-Muskeldystrophien (LGMD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.360,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_295\">\n                    <td style=\"\">ECHS1<\/td>\n                    <td style=\"\">Leigh-Syndrom mit Leukodystrophie, infantile nekrotisierende subakute Encephalomyelopathie mit Leukodystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">873,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_296\">\n                    <td style=\"\">EFEMP1<\/td>\n                    <td style=\"\">Famili\u00e4re Drusen<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.482,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_297\">\n                    <td style=\"\">EFHC1<\/td>\n                    <td style=\"\">Juvenile Myoklonus Epilepsie (JME)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.923,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_298\">\n                    <td style=\"\">EFHC1<\/td>\n                    <td style=\"\">Risikofaktor f\u00fcr eine  juvenile myoklonische Epilepsie 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.923,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_299\">\n                    <td style=\"\">EFNB1<\/td>\n                    <td style=\"\">kranio-fronto-nasale Dysplasie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_300\">\n                    <td style=\"\">EGF<\/td>\n                    <td style=\"\">Renale Hypomagnesi\u00e4mieTyp  4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.624,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_301\">\n                    <td style=\"\">EGR2<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit Typ 1D<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.470,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_302\">\n                    <td style=\"\">EGR2<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit Typ 4E<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.470,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_303\">\n                    <td style=\"\">ELANE<\/td>\n                    <td style=\"\">Schwer kongentiale, autosomal-dominante Neutropenie 1<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">804,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_304\">\n                    <td style=\"\">ELANE<\/td>\n                    <td style=\"\">Zyklische Neutropenie<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">804,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_305\">\n                    <td style=\"\">ELOVL4<\/td>\n                    <td style=\"\">Stargardt Krankheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">945,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_306\">\n                    <td style=\"\">EMX2<\/td>\n                    <td style=\"\">Schizenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">759,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_307\">\n                    <td style=\"\">EMX2<\/td>\n                    <td style=\"\">Schizenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">759,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_308\">\n                    <td style=\"\">ENG<\/td>\n                    <td style=\"\">Heredit\u00e4re h\u00e4morrhagische Teleangiektasie (HHT), Typ 1; Morbus Osler<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.097,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_309\">\n                    <td style=\"\">EOMES<\/td>\n                    <td style=\"\">Mikrocephalie Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.118,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_310\">\n                    <td style=\"\">EP300<\/td>\n                    <td style=\"\">Rubinstein-Taybi Syndrom 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">7.245,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_311\">\n                    <td style=\"\">EPM2A<\/td>\n                    <td style=\"\">Lafora Krankheit<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">996,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_312\">\n                    <td style=\"\">ERCC1<\/td>\n                    <td style=\"\">Xeroderma pigmentosum<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">972,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_313\">\n                    <td style=\"\">ERCC2<\/td>\n                    <td style=\"\">Xeroderma pigmentosum<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.490,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_314\">\n                    <td style=\"\">ERCC4<\/td>\n                    <td style=\"\">Xeroderma pigmentosum<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.889,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_315\">\n                    <td style=\"\">ERCC5<\/td>\n                    <td style=\"\">Xeroderma pigmentosum<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.561,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_316\">\n                    <td style=\"\">ERCC6<\/td>\n                    <td style=\"\">Cockayne-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.482,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_317\">\n                    <td style=\"\">ERCC6<\/td>\n                    <td style=\"\">Altersabh\u00e4ngige Makuladegeneration<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.482,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_318\">\n                    <td style=\"\">ERCC8<\/td>\n                    <td style=\"\">Cockayne-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.248,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_319\">\n                    <td style=\"\">ETFA<\/td>\n                    <td style=\"\">Multiple Acyl-CoA-Dehydrogenase-Mangel (MADD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.221,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_320\">\n                    <td style=\"\">ETFA<\/td>\n                    <td style=\"\">Multipler Acyl-CoA-Dehydrogenase-Mangel (MADD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.221,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_321\">\n                    <td style=\"\">ETFB<\/td>\n                    <td style=\"\">Multiple Acyl-CoA-Dehydrogenase-Mangel (MADD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_322\">\n                    <td style=\"\">ETFB<\/td>\n                    <td style=\"\">Multipler Acyl-CoA-Dehydrogenase-Mangel (MADD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_323\">\n                    <td style=\"\">ETFDH<\/td>\n                    <td style=\"\">Multipler Acyl-CoA-Dehydrogenase-Mangel (MADD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.857,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_324\">\n                    <td style=\"\">ETFDH<\/td>\n                    <td style=\"\">Multiple Acyl-CoA-Dehydrogenase-Mangel (MADD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.857,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_325\">\n                    <td style=\"\">ETHE1<\/td>\n                    <td style=\"\">Ethylmalons\u00e4ure-Enzephalopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">783,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_326\">\n                    <td style=\"\">EXOSC3<\/td>\n                    <td style=\"\">Pontozerebell\u00e4re Hypoplasie Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">828,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_327\">\n                    <td style=\"\">EXT1<\/td>\n                    <td style=\"\">Multiple Exostosen<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.241,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_328\">\n                    <td style=\"\">EXT2<\/td>\n                    <td style=\"\">Multiple Exostosen<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.256,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_329\">\n                    <td style=\"\">F12<\/td>\n                    <td style=\"\">Angi\u00f6dem, erblich, Type III<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.848,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_330\">\n                    <td style=\"\">F12<\/td>\n                    <td style=\"\">kongenitaler Faktor XII-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.848,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_331\">\n                    <td style=\"\">F12<\/td>\n                    <td style=\"\">Heredit\u00e4res Angio\u00f6dem Typ 3 (Mutation im Gerinnungsfaktor XII; Exon 9 des F12-Gens)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.848,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_332\">\n                    <td style=\"\">F2<\/td>\n                    <td style=\"\">kongenitaler Faktor II-Mangel\/Prothrombin-Mangel (Dysprothrombin\u00e4mie\/Hypoprothrombin\u00e4mie)<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.869,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_333\">\n                    <td style=\"\">F2<\/td>\n                    <td style=\"\">Thrombophilie (20210G&gt;A-\/c.*97G&gt;A-Mutation)<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.869,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_334\">\n                    <td style=\"\">F5<\/td>\n                    <td style=\"\">Gerinnungsfaktor V-Leiden-Mutation\/APC-Resistenz<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.675,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_335\">\n                    <td style=\"\">F9<\/td>\n                    <td style=\"\">H\u00e4mophilie B<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.386,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_336\">\n                    <td style=\"\">FA2H<\/td>\n                    <td style=\"\">Spastische Paraplegie Typ 35<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.119,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_337\">\n                    <td style=\"\">FA2H<\/td>\n                    <td style=\"\">Leukodystrophie - spastische Paraplegie - Dystonie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.119,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_338\">\n                    <td style=\"\">FAH<\/td>\n                    <td style=\"\">Tyrosin\u00e4mie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.260,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_339\">\n                    <td style=\"\">FANCC<\/td>\n                    <td style=\"\">Fanconi anemia, complementation group C; FANCC<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.677,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_340\">\n                    <td style=\"\">FANCG<\/td>\n                    <td style=\"\">Fanconi-An\u00e4mie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.869,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_341\">\n                    <td style=\"\">FAS<\/td>\n                    <td style=\"\">Autoimmunes lymphoproliferatives Syndrom Typ 1A<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.008,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_342\">\n                    <td style=\"\">FGA<\/td>\n                    <td style=\"\">Heredit\u00e4re Amyloidose (FGA- und TTR-Gen)<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.601,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_343\">\n                    <td style=\"\">FGD1<\/td>\n                    <td style=\"\">Aarskog-Scott Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.886,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_344\">\n                    <td style=\"\">FGD1<\/td>\n                    <td style=\"\">Mentale Retardierung, x-gekoppelt, Syndrom 16<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.886,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_345\">\n                    <td style=\"\">FGF14<\/td>\n                    <td style=\"\">Ataxie, spinozerebell\u00e4re, Typ 27<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">759,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_346\">\n                    <td style=\"\">FGF23<\/td>\n                    <td style=\"\">Tumor\u00f6se Kalzinose, hyperkalz\u00e4mische (Famili\u00e4re hyperphosphat\u00e4mische tumorale Kalzinose\/Hyperphosphat\u00e4mische Hyperostose-Syndrom)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">756,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_347\">\n                    <td style=\"\">FGF23<\/td>\n                    <td style=\"\">Hypophosphat\u00e4mische Rachitis, autosomal dominant<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">756,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_348\">\n                    <td style=\"\">FGF23<\/td>\n                    <td style=\"\">Osteomalazie, tumor-induziert<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">756,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_349\">\n                    <td style=\"\">FGF8<\/td>\n                    <td style=\"\">Hypogonadotroper Hypogonadismus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">735,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_350\">\n                    <td style=\"\">FGF8<\/td>\n                    <td style=\"\">Holoprosenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">735,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_351\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">Kraniosynostose, unspezifisch<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_352\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">FGFR2-abh\u00e4ngige Dysplasie mit gekr\u00fcmmten Knochen<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_353\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">Pfeiffer Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_354\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">Skaphozephalie-Syndrom, famili\u00e4res, Typ McGillivray<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_355\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">Scaphocephalie und Axenfeld-Rieger Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_356\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">Apert Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_357\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">Jackson-Weiss Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_358\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">Akrozephalosyndaktylie Typ 5 (Kraniofaziale-skelettale dermatologische Dysplasie (Akrozephalosyndaktylie Typ 5)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_359\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">Cutis gyrata - Acanthosis nigricans \u2013 Kraniosynostose (Beare-Stevenson Syndrom )<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_360\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">LADD Syndrom \/ Lakrimo-aurikulo-dento-digitales Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_361\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">Crouzon Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_362\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">Saethre-Chotzen-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_363\">\n                    <td style=\"\">FGFR2<\/td>\n                    <td style=\"\">Antley-Bixler-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.469,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_364\">\n                    <td style=\"\">FGFR3<\/td>\n                    <td style=\"\">Achondroplasie<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_365\">\n                    <td style=\"\">FGFR3<\/td>\n                    <td style=\"\">THANATOPHORIC DYSPLASIA, TYPE II; TD2<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_366\">\n                    <td style=\"\">FGFR3<\/td>\n                    <td style=\"\">CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME; CATSHLS<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_367\">\n                    <td style=\"\">FGFR3<\/td>\n                    <td style=\"\">THANATOPHORIC DYSPLASIA, TYPE I; TD1<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_368\">\n                    <td style=\"\">FGFR3<\/td>\n                    <td style=\"\">Saddan Syndrom<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_369\">\n                    <td style=\"\">FGFR3<\/td>\n                    <td style=\"\">Crouzon-Syndrom - Acanthosis nigricans (Crouzon-dermato-skeletales-Syndrom)<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_370\">\n                    <td style=\"\">FGFR3<\/td>\n                    <td style=\"\">Lakrimo-aurikulo-dento-digitales Syndrom<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_371\">\n                    <td style=\"\">FGFR3<\/td>\n                    <td style=\"\">Hypochondroplasie<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_372\">\n                    <td style=\"\">FGFR3<\/td>\n                    <td style=\"\">Crouzon Syndrom<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_373\">\n                    <td style=\"\">FGFR3<\/td>\n                    <td style=\"\">Muenke-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_374\">\n                    <td style=\"\">FLNA<\/td>\n                    <td style=\"\">Periventrikul\u00e4re nodul\u00e4re Heterotopie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">7.944,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_375\">\n                    <td style=\"\">FLT4<\/td>\n                    <td style=\"\">Lymph\u00f6dem, heredit\u00e4res, Typ I<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.092,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_376\">\n                    <td style=\"\">FLT4<\/td>\n                    <td style=\"\">Heredit\u00e4res Lymph\u00f6dem Typ I (Mutation in Exons 17-25 des FLT4-Gens)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.092,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_377\">\n                    <td style=\"\">FLT4<\/td>\n                    <td style=\"\">kapill\u00e4re H\u00e4mangiom, somatisch<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.092,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_378\">\n                    <td style=\"\">FLVCR1<\/td>\n                    <td style=\"\">Hinterstrangataxie - Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.668,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_379\">\n                    <td style=\"\">FLVCR2<\/td>\n                    <td style=\"\">Fowler Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.581,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_380\">\n                    <td style=\"\">FOLR1<\/td>\n                    <td style=\"\">Neurodegeneratives Syndrom durch zerebrale Folattransportst\u00f6rung<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">774,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_381\">\n                    <td style=\"\">FOXC1<\/td>\n                    <td style=\"\">Peters-Anomalie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.662,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_382\">\n                    <td style=\"\">FOXC1<\/td>\n                    <td style=\"\">Rieger-Axenfeld-Anomalie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.662,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_383\">\n                    <td style=\"\">FOXE1<\/td>\n                    <td style=\"\">Bamforth-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.122,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_384\">\n                    <td style=\"\">FOXG1<\/td>\n                    <td style=\"\">atypisches Rett-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.470,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_385\">\n                    <td style=\"\">FRAS1<\/td>\n                    <td style=\"\">Fraser-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">12.039,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_386\">\n                    <td style=\"\">FREM1<\/td>\n                    <td style=\"\">BIFID NOSE WITH OR WITHOUT ANORECTAL AND RENAL ANOMALIES; BNAR<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.540,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_387\">\n                    <td style=\"\">FREM1<\/td>\n                    <td style=\"\">MANITOBA OCULOTRICHOANAL SYNDROME; MOTA<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.540,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_388\">\n                    <td style=\"\">FREM1<\/td>\n                    <td style=\"\">TRIGONOCEPHALY 2; TRIGNO2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.540,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_389\">\n                    <td style=\"\">FSCN2<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.551,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_390\">\n                    <td style=\"\">FSHB<\/td>\n                    <td style=\"\">Hypogonadotropher Hypogonadismus 24 ohne Anosmie \/ Follikelstimulierendes-Hormon-Mangel, isolierter<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">390,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_391\">\n                    <td style=\"\">FTL<\/td>\n                    <td style=\"\">Neurodegeneration mit Eisenablagerung im Gehirn (NBIA)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">528,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_392\">\n                    <td style=\"\">FTL<\/td>\n                    <td style=\"\">Hyperferritin\u00e4mie-Katarakt-Syndrom (Mutation im IRE des FTL-Gens)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">528,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_393\">\n                    <td style=\"\">FUS<\/td>\n                    <td style=\"\">Amyotrophe Lateralsklerose (ALS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.581,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_394\">\n                    <td style=\"\">FZD4<\/td>\n                    <td style=\"\">Famili\u00e4re exsudativen Retinopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.614,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_395\">\n                    <td style=\"\">G6PC1<\/td>\n                    <td style=\"\">Glycogen Storage Disease Type Ia<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.074,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_396\">\n                    <td style=\"\">G6PC3<\/td>\n                    <td style=\"\">Dursun Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_397\">\n                    <td style=\"\">G6PC3<\/td>\n                    <td style=\"\">Schwer kongentiale, autosomal rezessive, Neutropenie 4, durch G6PC3-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_398\">\n                    <td style=\"\">GAA<\/td>\n                    <td style=\"\">Glykogen-Speicherkrankheit durch Saure-Maltase-Mangel<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.859,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_399\">\n                    <td style=\"\">GABRA1<\/td>\n                    <td style=\"\">Juvenile Myoklonus Epilepsie (JME)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.371,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_400\">\n                    <td style=\"\">GABRB3<\/td>\n                    <td style=\"\">Absencenepilepsie der Kindheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.590,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_401\">\n                    <td style=\"\">GABRD<\/td>\n                    <td style=\"\">Generalisierte Epilepsie mit Fieberkr\u00e4mpfen Plus (GEFS+)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.359,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_402\">\n                    <td style=\"\">GABRD<\/td>\n                    <td style=\"\">Generalisierte Epilepsie mit Fieberkr\u00e4mpfen plus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.359,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_403\">\n                    <td style=\"\">GABRD<\/td>\n                    <td style=\"\">Juvenile Myoklonus Epilepsie (JME)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.359,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_404\">\n                    <td style=\"\">GABRG2<\/td>\n                    <td style=\"\">Absencenepilepsie der Kindheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.548,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_405\">\n                    <td style=\"\">GALC<\/td>\n                    <td style=\"\">Morbus Krabbe<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.058,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_406\">\n                    <td style=\"\">GALNT3<\/td>\n                    <td style=\"\">Tumorale hyperkalz\u00e4mische Kalzinose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.902,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_407\">\n                    <td style=\"\">GAMT<\/td>\n                    <td style=\"\">Guanidinoacetat-Methyltransferase-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">810,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_408\">\n                    <td style=\"\">GARS1<\/td>\n                    <td style=\"\">distale heredit\u00e4re motorische Neuropathie, Typ 5<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.238,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_409\">\n                    <td style=\"\">GARS1<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit Typ 2D<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.238,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_410\">\n                    <td style=\"\">GATA1<\/td>\n                    <td style=\"\">Thrombozytopenie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.257,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_411\">\n                    <td style=\"\">GATA2<\/td>\n                    <td style=\"\">Emberger Syndrom (Taubheit-Lymph\u00f6dem-Leuk\u00e4mie-Syndrom)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.725,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_412\">\n                    <td style=\"\">GATA2<\/td>\n                    <td style=\"\">Immunodefizienz 21<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.725,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_413\">\n                    <td style=\"\">GATA6<\/td>\n                    <td style=\"\">Atrioventrikul\u00e4rer Septumdefekt \/ Atrioventrikularkanaldefekt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.788,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_414\">\n                    <td style=\"\">GATA6<\/td>\n                    <td style=\"\">Fallot-Tetralogie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.788,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_415\">\n                    <td style=\"\">GATA6<\/td>\n                    <td style=\"\">Atriumseptumdefekt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.788,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_416\">\n                    <td style=\"\">GATA6<\/td>\n                    <td style=\"\">Pankreashypoplasie - Diabetes - Herzkrankheit, kongenital (Yorifuji-Okuno-Syndrom)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.788,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_417\">\n                    <td style=\"\">GBA<\/td>\n                    <td style=\"\">Parkinson Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.611,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_418\">\n                    <td style=\"\">GBE1<\/td>\n                    <td style=\"\">Glykogenspeicherkrankheit Typ 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.109,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_419\">\n                    <td style=\"\">GCDH<\/td>\n                    <td style=\"\">Glutaryl-CoA-Dehydrogenase-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.569,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_420\">\n                    <td style=\"\">GCH1<\/td>\n                    <td style=\"\">Dopa-responsive Dystonie DYT5<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">753,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_421\">\n                    <td style=\"\">GCK<\/td>\n                    <td style=\"\">Hyperinsulin\u00e4mische Hypoglyk\u00e4mie, famili\u00e4r, 3 (Hyperinsulinismus durch Glukokinase-Mangel)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.461,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_422\">\n                    <td style=\"\">GCK<\/td>\n                    <td style=\"\">Diabetes mellitus in der Schwangerschaft<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.461,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_423\">\n                    <td style=\"\">GCK<\/td>\n                    <td style=\"\">Diabetes mellitus, nicht-insulin-abh\u00e4ngig, sp\u00e4ter Ausbruch<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.461,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_424\">\n                    <td style=\"\">GCK<\/td>\n                    <td style=\"\">MODY, Typ II<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.461,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_425\">\n                    <td style=\"\">GCK<\/td>\n                    <td style=\"\">Diabetes mellitus, permanent neonatal<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.461,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_426\">\n                    <td style=\"\">GCNT2<\/td>\n                    <td style=\"\">heredit\u00e4re Katarakt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.209,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_427\">\n                    <td style=\"\">GCSH<\/td>\n                    <td style=\"\">Nicht-ketotische Hyperglyzin\u00e4mie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">522,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_428\">\n                    <td style=\"\">GDAP1<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit Typ 4A<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.155,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_429\">\n                    <td style=\"\">GDAP1<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit Typ 2H<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.155,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_430\">\n                    <td style=\"\">GDAP1<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit Typ 2K<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.155,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_431\">\n                    <td style=\"\">GDF2<\/td>\n                    <td style=\"\">Heredit\u00e4re h\u00e4morrhagische Teleangiektasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.290,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_432\">\n                    <td style=\"\">GDF9<\/td>\n                    <td style=\"\">Primary Ovarian Failure<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.365,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_433\">\n                    <td style=\"\">GFAP<\/td>\n                    <td style=\"\">Alexander Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.419,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_434\">\n                    <td style=\"\">GFER<\/td>\n                    <td style=\"\">Kongenitale Katarakt-progressive Muskelhypotonie-H\u00f6rverlust-Entwicklungsverz\u00f6gerung-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">618,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_435\">\n                    <td style=\"\">GJA1<\/td>\n                    <td style=\"\">Syndaktylie Typ 3 (SD3)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.149,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_436\">\n                    <td style=\"\">GJA1<\/td>\n                    <td style=\"\">Okulo-dento-digitale Dysplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.149,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_437\">\n                    <td style=\"\">GJA1<\/td>\n                    <td style=\"\">Hypoplastische Linksherz-Syndrom (HLHS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.149,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_438\">\n                    <td style=\"\">GJB1<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth X-Linked<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">852,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_439\">\n                    <td style=\"\">GJB2<\/td>\n                    <td style=\"\">nicht-syndromale sensorineurale autosomal-dominante Schwerh\u00f6rigkeit Typ DFNA<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">681,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_440\">\n                    <td style=\"\">GJB2<\/td>\n                    <td style=\"\">Autosomal-rezessive nicht-syndromale sensorineurale Schwerh\u00f6rigkeit Typ DFNB<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">681,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_441\">\n                    <td style=\"\">GJB2<\/td>\n                    <td style=\"\">Vohwinkel Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">681,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_442\">\n                    <td style=\"\">GJB2<\/td>\n                    <td style=\"\">Autosomal-dominante nicht-syndromale sensorineurale Schwerh\u00f6rigkeit Typ DFNA<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">681,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_443\">\n                    <td style=\"\">GJB3<\/td>\n                    <td style=\"\">Erythrokeratoderma variabilis Typ Mendes da Costa (EKV)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">813,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_444\">\n                    <td style=\"\">GJB6<\/td>\n                    <td style=\"\">Autosomal-dominante nicht-syndromale sensorineurale Schwerh\u00f6rigkeit Typ DFNA<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">786,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_445\">\n                    <td style=\"\">GJB6<\/td>\n                    <td style=\"\">nicht-syndromale sensorineurale autosomal-dominante Schwerh\u00f6rigkeit Typ DFNA<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">786,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_446\">\n                    <td style=\"\">GJC2<\/td>\n                    <td style=\"\">Pelizaeus-Merzbacher-\u00e4hnliche Krankheit mit GJC2-Genmutationen<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.320,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_447\">\n                    <td style=\"\">GJC2<\/td>\n                    <td style=\"\">Spastische Paraplegie Typ 44<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.320,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_448\">\n                    <td style=\"\">GLA<\/td>\n                    <td style=\"\">Fabry Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.413,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_449\">\n                    <td style=\"\">GLB1<\/td>\n                    <td style=\"\">Mukopolysaccharidose Typ 4B<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.178,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_450\">\n                    <td style=\"\">GLB1<\/td>\n                    <td style=\"\">GM1-Gangliosidose Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.178,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_451\">\n                    <td style=\"\">GLDC<\/td>\n                    <td style=\"\">Nicht-ketotische Hyperglyzin\u00e4mie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.063,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_452\">\n                    <td style=\"\">GLE1<\/td>\n                    <td style=\"\">Letales kongenitales Kontraktursyndrom 1 (LCCS1)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.124,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_453\">\n                    <td style=\"\">GLE1<\/td>\n                    <td style=\"\">Letale Arthrogrypose mit Vorderhornerkrankung (LAAHD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.124,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_454\">\n                    <td style=\"\">GLI2<\/td>\n                    <td style=\"\">Holoprosencephalie 9<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.761,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_455\">\n                    <td style=\"\">GLI2<\/td>\n                    <td style=\"\">Culler Jones Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.761,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_456\">\n                    <td style=\"\">GLI3<\/td>\n                    <td style=\"\">Greig Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.743,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_457\">\n                    <td style=\"\">GLRA1<\/td>\n                    <td style=\"\">heredit\u00e4re Hyperekplexie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.374,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_458\">\n                    <td style=\"\">GLRB<\/td>\n                    <td style=\"\">heredit\u00e4re Hyperekplexie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.494,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_459\">\n                    <td style=\"\">GLUL<\/td>\n                    <td style=\"\">kongenitale Hirnfehlbildung durch Glutamin-Synthetase-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.524,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_460\">\n                    <td style=\"\">GNA11<\/td>\n                    <td style=\"\">Hypokalziurische Hyperkalz\u00e4mie, Typ II<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.080,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_461\">\n                    <td style=\"\">GNA11<\/td>\n                    <td style=\"\">Hypokalz\u00e4mie, autosomal dominant 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.080,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_462\">\n                    <td style=\"\">GNAQ<\/td>\n                    <td style=\"\">Sturge-Weber Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.080,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_463\">\n                    <td style=\"\">GNAQ<\/td>\n                    <td style=\"\">Kapill\u00e4re Fehlbildungen, kongenital, 1, somatisch<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.080,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_464\">\n                    <td style=\"\">GNAT2<\/td>\n                    <td style=\"\">Achromatopsie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.065,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_465\">\n                    <td style=\"\">GNPTAB<\/td>\n                    <td style=\"\">Mukolipidose\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.771,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_466\">\n                    <td style=\"\">GNPTG<\/td>\n                    <td style=\"\">Mukolipidose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">966,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_467\">\n                    <td style=\"\">GNRHR<\/td>\n                    <td style=\"\">Hypogonadotroper Hypogonadismus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">987,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_468\">\n                    <td style=\"\">GNS<\/td>\n                    <td style=\"\">Mukopolysaccharidose Typ IIID (Sanfilippo D)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.659,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_469\">\n                    <td style=\"\">GOSR2<\/td>\n                    <td style=\"\">Myoklonus Epilepsie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">774,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_470\">\n                    <td style=\"\">GPHN<\/td>\n                    <td style=\"\">heredit\u00e4re Hyperekplexie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.310,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_471\">\n                    <td style=\"\">GPHN<\/td>\n                    <td style=\"\">Molybd\u00e4n-Cofaktor-Defizienz C (Sulfitoxidase-Mangel durch Molybd\u00e4n-Kofaktor-Mangel Typ C)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.310,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_472\">\n                    <td style=\"\">GPR143<\/td>\n                    <td style=\"\">Okul\u00e4rer Albinismus X-linked<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.215,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_473\">\n                    <td style=\"\">GPSM2<\/td>\n                    <td style=\"\">Chudley-McCullough Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.106,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_474\">\n                    <td style=\"\">GRIN2A<\/td>\n                    <td style=\"\">Fr\u00fch-beginnende epileptische Enzephalopathie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.395,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_475\">\n                    <td style=\"\">GRN<\/td>\n                    <td style=\"\">Frontotemporale Demenz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.782,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_476\">\n                    <td style=\"\">GSN<\/td>\n                    <td style=\"\">Agel-Amyloidose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.349,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_477\">\n                    <td style=\"\">GSS<\/td>\n                    <td style=\"\">Glutathionsynthetase-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.425,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_478\">\n                    <td style=\"\">GUCA1A<\/td>\n                    <td style=\"\">Zapfen-St\u00e4bchen-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">606,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_479\">\n                    <td style=\"\">GUCY2D<\/td>\n                    <td style=\"\">Leber Congenitale Amaurose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.312,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_480\">\n                    <td style=\"\">GYS2<\/td>\n                    <td style=\"\">Glykogenspeicherkrankheit durch hepatischen Glykogensynthase Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.112,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_481\">\n                    <td style=\"\">HAMP<\/td>\n                    <td style=\"\">H\u00e4mochromatose Typ 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">255,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_482\">\n                    <td style=\"\">HAX1<\/td>\n                    <td style=\"\">Schwer kongentiale, autosomal rezessive, Neutropenie 3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">840,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_483\">\n                    <td style=\"\">HCN4<\/td>\n                    <td style=\"\">Sick Sinus Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.612,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_484\">\n                    <td style=\"\">HCRT<\/td>\n                    <td style=\"\">Narkolepsie ohne Kataplexie \/ Narkolepsie-Kataplexie-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">396,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_485\">\n                    <td style=\"\">HDAC8<\/td>\n                    <td style=\"\">Cornelia de Lange Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.245,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_486\">\n                    <td style=\"\">HESX1<\/td>\n                    <td style=\"\">Septo-optische Dysplasie (SOD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">558,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_487\">\n                    <td style=\"\">HEXA<\/td>\n                    <td style=\"\">GM2-Gangliosidose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.623,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_488\">\n                    <td style=\"\">HEXA<\/td>\n                    <td style=\"\">Tay-Sachs-Krankheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.623,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_489\">\n                    <td style=\"\">HFE<\/td>\n                    <td style=\"\">H\u00e4mochromatose Typ 4<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">1.047,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_490\">\n                    <td style=\"\">HFE<\/td>\n                    <td style=\"\">H\u00e4mochromatose Typ 1 (C282Y- und H63D-Mut.; Seq. n. R\u00fccksprache)<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">1.047,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_491\">\n                    <td style=\"\">HGSNAT<\/td>\n                    <td style=\"\">Retinitis pigmentosa 73<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.908,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_492\">\n                    <td style=\"\">HGSNAT<\/td>\n                    <td style=\"\">Mucopolysaccharidose Typ IIIC (Sanfilippo C)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.908,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_493\">\n                    <td style=\"\">HINT1<\/td>\n                    <td style=\"\">Axonale Neuropathie mit Neuromyotonie, autosomal-rezessiv<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">381,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_494\">\n                    <td style=\"\">HJV<\/td>\n                    <td style=\"\">H\u00e4mochromatose Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.281,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_495\">\n                    <td style=\"\">HNF1A<\/td>\n                    <td style=\"\">MODY-Diabetes (Maturity-Onset Diabetes of the Young Typ 3)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.917,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_496\">\n                    <td style=\"\">HNF1B<\/td>\n                    <td style=\"\">Diabetes mellitus<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.674,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_497\">\n                    <td style=\"\">HNF1B<\/td>\n                    <td style=\"\">Renale Zysten und Diabetes-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.674,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_498\">\n                    <td style=\"\">HNF4A<\/td>\n                    <td style=\"\">MODY, Typ I<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.425,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_499\">\n                    <td style=\"\">HNF4A<\/td>\n                    <td style=\"\">Renale Zysten und Diabetes-Syndrom (MODY 5)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.425,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_500\">\n                    <td style=\"\">HOGA1<\/td>\n                    <td style=\"\">Prim\u00e4re Hyperoxalurie, Typ 3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">984,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_501\">\n                    <td style=\"\">HOXD13<\/td>\n                    <td style=\"\">Brachydaktylie, Typ E<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.032,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_502\">\n                    <td style=\"\">HOXD13<\/td>\n                    <td style=\"\">Syndaktylie, Typ V<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.032,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_503\">\n                    <td style=\"\">HOXD13<\/td>\n                    <td style=\"\">Synpolydaktylie, Typ I<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.032,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_504\">\n                    <td style=\"\">HOXD13<\/td>\n                    <td style=\"\">Brachydaktylie-Syndaktylie Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.032,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_505\">\n                    <td style=\"\">HOXD13<\/td>\n                    <td style=\"\">Brachydaktylie, Typ D<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.032,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_506\">\n                    <td style=\"\">HRAS<\/td>\n                    <td style=\"\">Costello Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">570,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_507\">\n                    <td style=\"\">HSD11B1<\/td>\n                    <td style=\"\">Hyperandrogenismus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">879,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_508\">\n                    <td style=\"\">HSD17B10<\/td>\n                    <td style=\"\">17-Beta-Hydroxysteroid-Dehydrogenase-Defizienz \/ HSD10-Krankheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">786,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_509\">\n                    <td style=\"\">HSD17B4<\/td>\n                    <td style=\"\">D-bifunktionales Enzym-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.286,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_510\">\n                    <td style=\"\">HSD17B4<\/td>\n                    <td style=\"\">Perrault-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.286,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_511\">\n                    <td style=\"\">HSD3B7<\/td>\n                    <td style=\"\">Gallens\u00e4uresynthesedefekt, kongenitaler, Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.110,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_512\">\n                    <td style=\"\">HSF4<\/td>\n                    <td style=\"\">heredit\u00e4re Katarakt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.479,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_513\">\n                    <td style=\"\">HTRA1<\/td>\n                    <td style=\"\">CARASIL-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.443,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_514\">\n                    <td style=\"\">HTT<\/td>\n                    <td style=\"\">Huntington Disease, HD<\/td>\n                    <td style=\"\">Fragmentl\u00e4ngenanalyse<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">9.429,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_515\">\n                    <td style=\"\">IDS<\/td>\n                    <td style=\"\">Mukopolysaccharidose Typ 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.653,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_516\">\n                    <td style=\"\">IFIH1<\/td>\n                    <td style=\"\">Aicardi-Gouti\u00e8res-Syndrom 7<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.078,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_517\">\n                    <td style=\"\">IFIH1<\/td>\n                    <td style=\"\">Singleton-Merten-Dysplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.078,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_518\">\n                    <td style=\"\">IL1RAPL1<\/td>\n                    <td style=\"\">Mentale Retardierung, nicht syndromal, x-gekoppelt, 21\/34<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.091,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_519\">\n                    <td style=\"\">IL36RN<\/td>\n                    <td style=\"\">Generalisierte pustul\u00f6se Psoriasis<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">468,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_520\">\n                    <td style=\"\">IPMK<\/td>\n                    <td style=\"\">Heredit\u00e4rer neuroendokriner Tumor des D\u00fcnndarms<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.251,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_521\">\n                    <td style=\"\">IRF6<\/td>\n                    <td style=\"\">Van der Woude-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.404,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_522\">\n                    <td style=\"\">ISCU<\/td>\n                    <td style=\"\">Heredit\u00e4re Myopathie mit Laktatazidose durch ISCU-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">504,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_523\">\n                    <td style=\"\">ITM2B<\/td>\n                    <td style=\"\">Famili\u00e4re Demenz \/ Amyloidose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">801,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_524\">\n                    <td style=\"\">ITM2B<\/td>\n                    <td style=\"\">Netzhautdystrophie mit Dysfunktion der inneren Retina und Ganglienzellanomalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">801,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_525\">\n                    <td style=\"\">IYD<\/td>\n                    <td style=\"\">Schilddr\u00fcsen Dyshormonogenese 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">882,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_526\">\n                    <td style=\"\">JAG1<\/td>\n                    <td style=\"\">Alagille Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.657,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_527\">\n                    <td style=\"\">JAG1<\/td>\n                    <td style=\"\">Fallot-Tetralogie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.657,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_528\">\n                    <td style=\"\">JAGN1<\/td>\n                    <td style=\"\">Schwer kongentiale, autosomal rezessive, Neutropenie 6<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">552,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_529\">\n                    <td style=\"\">JAK2<\/td>\n                    <td style=\"\">Budd-Chiari-Syndrom (BCS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.399,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_530\">\n                    <td style=\"\">JPH3<\/td>\n                    <td style=\"\">Huntington disease-like 2 (HDL2)<\/td>\n                    <td style=\"\">Fragmentl\u00e4ngenanalyse<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.247,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_531\">\n                    <td style=\"\">KCNA1<\/td>\n                    <td style=\"\">episodische Ataxie Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.488,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_532\">\n                    <td style=\"\">KCNC3<\/td>\n                    <td style=\"\">Spinozerebell\u00e4re Ataxie Typ 13<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.307,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_533\">\n                    <td style=\"\">KCND3<\/td>\n                    <td style=\"\">Ataxie, spinozerebell\u00e4re, Typ 19<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.968,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_534\">\n                    <td style=\"\">KCND3<\/td>\n                    <td style=\"\">Brugada-Syndrom 9<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.968,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_535\">\n                    <td style=\"\">KCNE1<\/td>\n                    <td style=\"\">Romano-Ward Long-QT-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">390,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_536\">\n                    <td style=\"\">KCNE1<\/td>\n                    <td style=\"\">Jervell-und-Lange-Nielsen-Syndrom (Long-QT-Syndrom)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">390,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_537\">\n                    <td style=\"\">KCNE3<\/td>\n                    <td style=\"\">Brugada-Syndrom 6<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">312,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_538\">\n                    <td style=\"\">KCNJ10<\/td>\n                    <td style=\"\">Enlarged vestibular aqueduct, digenic<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.140,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_539\">\n                    <td style=\"\">KCNJ10<\/td>\n                    <td style=\"\">SeSAME-Syndrom \/ EAST-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.140,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_540\">\n                    <td style=\"\">KCNJ2<\/td>\n                    <td style=\"\">Short QT Syndrom, famili\u00e4res<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.284,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_541\">\n                    <td style=\"\">KCNJ2<\/td>\n                    <td style=\"\">Andersen Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.284,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_542\">\n                    <td style=\"\">KCNJ2<\/td>\n                    <td style=\"\">Vorhofflimmern, famili\u00e4res<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.284,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_543\">\n                    <td style=\"\">KCNJ5<\/td>\n                    <td style=\"\">Famili\u00e4res Hyperaldosteronismus, Typ III<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.260,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_544\">\n                    <td style=\"\">KCNJ8<\/td>\n                    <td style=\"\">Cantu Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.275,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_545\">\n                    <td style=\"\">KCNK18<\/td>\n                    <td style=\"\">Risikofaktor f\u00fcr Migr\u00e4ne, mit oder ohne Aura<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.155,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_546\">\n                    <td style=\"\">KCNMA1<\/td>\n                    <td style=\"\">Generalisierte Epilepsie mit paroxysmaler Dyskinesie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.711,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_547\">\n                    <td style=\"\">KCNQ2<\/td>\n                    <td style=\"\">Benigne neonatale Epilepsie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.673,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_548\">\n                    <td style=\"\">KCNQ3<\/td>\n                    <td style=\"\">Benigne neonatale Epilepsie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.619,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_549\">\n                    <td style=\"\">KCNT1<\/td>\n                    <td style=\"\">N\u00e4chtliche Frontallappen- Epilepsie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.708,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_550\">\n                    <td style=\"\">KCNT1<\/td>\n                    <td style=\"\">Epileptische Enzephalopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.708,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_551\">\n                    <td style=\"\">KCNV2<\/td>\n                    <td style=\"\">Zapfen-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.638,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_552\">\n                    <td style=\"\">KCTD17<\/td>\n                    <td style=\"\">Myoklonus-Dystonie-Syndrom 26<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">945,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_553\">\n                    <td style=\"\">KCTD7<\/td>\n                    <td style=\"\">progressive Myoklonusepilepsie, Typ 3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">870,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_554\">\n                    <td style=\"\">KIAA1549<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.853,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_555\">\n                    <td style=\"\">KIF1A<\/td>\n                    <td style=\"\">Spastische Paraplegie, Typ 30<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_556\">\n                    <td style=\"\">KIF1A<\/td>\n                    <td style=\"\">Heredit\u00e4re sensible und autonome Neuropathie Typ 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_557\">\n                    <td style=\"\">KIF1A<\/td>\n                    <td style=\"\">Mentale Retardierung<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_558\">\n                    <td style=\"\">KIF1B<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit Typ 2A1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.514,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_559\">\n                    <td style=\"\">KIF5A<\/td>\n                    <td style=\"\">Spastische Paraplegie Typ 10<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.120,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_560\">\n                    <td style=\"\">KIT<\/td>\n                    <td style=\"\">Piebaldismus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.934,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_561\">\n                    <td style=\"\">KIT<\/td>\n                    <td style=\"\">Famili\u00e4re gastrointestinale Stromatumoren<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.934,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_562\">\n                    <td style=\"\">KIT<\/td>\n                    <td style=\"\">Keimbahntumore<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.934,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_563\">\n                    <td style=\"\">KIT<\/td>\n                    <td style=\"\">Leuk\u00e4mie, akut myeloid<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.934,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_564\">\n                    <td style=\"\">KIT<\/td>\n                    <td style=\"\">Mastozytose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.934,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_565\">\n                    <td style=\"\">KMT2A<\/td>\n                    <td style=\"\">Wiedemann-Steiner-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">12.009,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_566\">\n                    <td style=\"\">KMT2A<\/td>\n                    <td style=\"\">lymphatische \/ myeloische Leuk\u00e4mie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">12.009,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_567\">\n                    <td style=\"\">KRAS<\/td>\n                    <td style=\"\">Noonan Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">570,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_568\">\n                    <td style=\"\">KRAS<\/td>\n                    <td style=\"\">Brustkrebs, somatisch<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">570,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_569\">\n                    <td style=\"\">KRT12<\/td>\n                    <td style=\"\">Meesmann-Hornhautdystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.485,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_570\">\n                    <td style=\"\">KRT16<\/td>\n                    <td style=\"\">Pachyonychia congenita, 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.422,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_571\">\n                    <td style=\"\">KRT16<\/td>\n                    <td style=\"\">Palmoplantarkeratose, nicht epidermolytisch, fokal<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.422,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_572\">\n                    <td style=\"\">KRT5<\/td>\n                    <td style=\"\">Epidermolysis bullosa simplex, rezessiv 1<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.773,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_573\">\n                    <td style=\"\">KRT5<\/td>\n                    <td style=\"\">Epidermolysis bullosa simplex, Dowling-Meara Typ<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.773,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_574\">\n                    <td style=\"\">KRT5<\/td>\n                    <td style=\"\">Epidermolysis bullosa simplex, allgemein<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.773,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_575\">\n                    <td style=\"\">KRT5<\/td>\n                    <td style=\"\">Epidermolysis bullosa simplex, lokal<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.773,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_576\">\n                    <td style=\"\">KRT5<\/td>\n                    <td style=\"\">Epidermolysis bullosa simplex-MP<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.773,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_577\">\n                    <td style=\"\">KRT5<\/td>\n                    <td style=\"\">Epidermolysis bullosa simplex, Weber-Cockayne Typ<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.773,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_578\">\n                    <td style=\"\">KRT5<\/td>\n                    <td style=\"\">Epidermylysis bullosa simplex-MCR<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.773,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_579\">\n                    <td style=\"\">KRT5<\/td>\n                    <td style=\"\">Epidermolysis bullosa simplex, Koebner Typ<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.773,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_580\">\n                    <td style=\"\">KRT6C<\/td>\n                    <td style=\"\">Autosomal-dominante fokale nicht-epidermolytische Palmoplantarkeratose mit Blasenbildung an den F\u00fc\u00dfen<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.695,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_581\">\n                    <td style=\"\">L1CAM<\/td>\n                    <td style=\"\">CRASH Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.774,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_582\">\n                    <td style=\"\">L1CAM<\/td>\n                    <td style=\"\">Hydrozephalus mit Hirschsprungkrankheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.774,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_583\">\n                    <td style=\"\">L1CAM<\/td>\n                    <td style=\"\">MASA Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.774,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_584\">\n                    <td style=\"\">L1CAM<\/td>\n                    <td style=\"\">Hydrozephalus mit Stenose des Aquaeductus Sylvii<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.774,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_585\">\n                    <td style=\"\">L1CAM<\/td>\n                    <td style=\"\">Corpus callosum-Dysgenesie, komplizierte, X-chromosomale<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.774,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_586\">\n                    <td style=\"\">L1CAM<\/td>\n                    <td style=\"\">Hydrozephalus mit kongenitaler idiopathischer intestinaler Pseudoobstruktion<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.774,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_587\">\n                    <td style=\"\">L2HGDH<\/td>\n                    <td style=\"\">L-2-Hydroxyglutaryl-Azidurie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.392,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_588\">\n                    <td style=\"\">LAMA1<\/td>\n                    <td style=\"\">Poretti-Boltshauser Syndrom (Ataxie-Intelligenzminderung-okulomotorische Apraxie-zerebell\u00e4re Zysten-Syndrom)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">9.228,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_589\">\n                    <td style=\"\">LAMA2<\/td>\n                    <td style=\"\">Muskeldystrophie, kongenitale, Typ 1A<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">9.369,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_590\">\n                    <td style=\"\">LARS1<\/td>\n                    <td style=\"\">Akutes infantiles Leberversagen-multisystemische Beteiligung-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.531,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_591\">\n                    <td style=\"\">LBR<\/td>\n                    <td style=\"\">Greenberg-Dysplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.848,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_592\">\n                    <td style=\"\">LDLR<\/td>\n                    <td style=\"\">Autosomal dominante fam. Hypercholesterin\u00e4mie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.841,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_593\">\n                    <td style=\"\">LEP<\/td>\n                    <td style=\"\">Adipositas durch angeborenen Leptinmangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">504,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_594\">\n                    <td style=\"\">LGI1<\/td>\n                    <td style=\"\">Schl\u00e4fenlappenepilepsie\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.674,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_595\">\n                    <td style=\"\">LHCGR<\/td>\n                    <td style=\"\">Leydig-Zellen Adenom, somatisch, mit vorzeitiger Pupert\u00e4t<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.100,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_596\">\n                    <td style=\"\">LHCGR<\/td>\n                    <td style=\"\">Leydig-Zellen Hypoplasie mit Pseudohermaphroditismus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.100,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_597\">\n                    <td style=\"\">LHCGR<\/td>\n                    <td style=\"\">Leydig-Zellen Hypoplasie mit hypergonadotropen Hypogonadismus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.100,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_598\">\n                    <td style=\"\">LHCGR<\/td>\n                    <td style=\"\">Vorzeitige m\u00e4nnliche Pubert\u00e4t, famili\u00e4re Form<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.100,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_599\">\n                    <td style=\"\">LHCGR<\/td>\n                    <td style=\"\">LH-Resistenz durch komplette LH-Rezeptor Inaktivierung<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.100,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_600\">\n                    <td style=\"\">LHX3<\/td>\n                    <td style=\"\">Hypophysenhormondefizienz, kombiniert<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.209,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_601\">\n                    <td style=\"\">LMNA<\/td>\n                    <td style=\"\">Hutchinson-Gilford Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_602\">\n                    <td style=\"\">LMNA<\/td>\n                    <td style=\"\">Gliederg\u00fcrtelmuskeldystrophie Typ 1B<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_603\">\n                    <td style=\"\">LMNA<\/td>\n                    <td style=\"\">Famili\u00e4re partielle Lipodystrophie, 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_604\">\n                    <td style=\"\">LMNA<\/td>\n                    <td style=\"\">Emery-Dreifuss-Muskeldystrophie 3, AR<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_605\">\n                    <td style=\"\">LMNA<\/td>\n                    <td style=\"\">Emery-Dreifuss-Muskeldystrophie 2, AD<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_606\">\n                    <td style=\"\">LMNA<\/td>\n                    <td style=\"\">Restriktive Dermopathie, letal<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_607\">\n                    <td style=\"\">LMNA<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth, Typ2B1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_608\">\n                    <td style=\"\">LMNA<\/td>\n                    <td style=\"\">Muskeldystrophie, kongenitale, Typ 1A<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_609\">\n                    <td style=\"\">LMNA<\/td>\n                    <td style=\"\">Herz Hand Syndrom, slowenischer Typ<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_610\">\n                    <td style=\"\">LMNA<\/td>\n                    <td style=\"\">Malouf-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_611\">\n                    <td style=\"\">LMNA<\/td>\n                    <td style=\"\">Kardiomyopathie, dilatative, 1A<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_612\">\n                    <td style=\"\">LMNA<\/td>\n                    <td style=\"\">Mandibuloakrale Dysplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_613\">\n                    <td style=\"\">LMNB1<\/td>\n                    <td style=\"\">autosomal-dominante Leukodystrophie (im Erwachsenenalter beginnend)<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.761,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_614\">\n                    <td style=\"\">LMX1B<\/td>\n                    <td style=\"\">Nagel-Patella-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.221,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_615\">\n                    <td style=\"\">LPIN1<\/td>\n                    <td style=\"\">autosomal rezessive rezidivierende Myoglobinurie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.928,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_616\">\n                    <td style=\"\">LPIN2<\/td>\n                    <td style=\"\">Majeed Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.691,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_617\">\n                    <td style=\"\">LRAT<\/td>\n                    <td style=\"\">Leber Congenitale Amaurose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">693,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_618\">\n                    <td style=\"\">LRAT<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">693,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_619\">\n                    <td style=\"\">LRMDA<\/td>\n                    <td style=\"\">Okulokutaner Albinismus Typ VII<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">681,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_620\">\n                    <td style=\"\">LRP5<\/td>\n                    <td style=\"\">Hyperostosis corticalis generalisata<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.848,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_621\">\n                    <td style=\"\">LRP5<\/td>\n                    <td style=\"\">Van-Buchem Syndrom Typ 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.848,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_622\">\n                    <td style=\"\">LRP5<\/td>\n                    <td style=\"\">Osteoporose-Pseudogliom-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.848,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_623\">\n                    <td style=\"\">LRP5<\/td>\n                    <td style=\"\">Famili\u00e4re exsudativen Retinopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.848,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_624\">\n                    <td style=\"\">LRRK2<\/td>\n                    <td style=\"\">Parkinson Syndrom<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">7.584,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_625\">\n                    <td style=\"\">LYST<\/td>\n                    <td style=\"\">Chediak-Higashi Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">11.406,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_626\">\n                    <td style=\"\">LYZ<\/td>\n                    <td style=\"\">Amyloidose, renal<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">447,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_627\">\n                    <td style=\"\">MAGEL2<\/td>\n                    <td style=\"\">Schaaf-Yang Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.750,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_628\">\n                    <td style=\"\">MAN2B1<\/td>\n                    <td style=\"\">Alpha-Mannosidose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.036,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_629\">\n                    <td style=\"\">MAPK10<\/td>\n                    <td style=\"\">Lennox-Gastaut-Syndrom (LGS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.656,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_630\">\n                    <td style=\"\">MAPT<\/td>\n                    <td style=\"\">Frontotemporale Demenz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.502,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_631\">\n                    <td style=\"\">MARS2<\/td>\n                    <td style=\"\">Spastische Ataxie mit Leukoenzephalopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.782,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_632\">\n                    <td style=\"\">MASP1<\/td>\n                    <td style=\"\">Kranio-fazio-ulnar-renales Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.187,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_633\">\n                    <td style=\"\">MATN3<\/td>\n                    <td style=\"\">Multiple epiphys\u00e4re Dysplasie\u00a0<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.461,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_634\">\n                    <td style=\"\">MBD5<\/td>\n                    <td style=\"\">Mentale Retardierung, autosomal dominant 1<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.184,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_635\">\n                    <td style=\"\">MC1R<\/td>\n                    <td style=\"\">Okulokutaner Albinismus, Typ II, modifier of<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">954,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_636\">\n                    <td style=\"\">MC1R<\/td>\n                    <td style=\"\">Melanoma, cutaneous malignant, 5<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">954,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_637\">\n                    <td style=\"\">MC1R<\/td>\n                    <td style=\"\">UV-induced skin damage<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">954,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_638\">\n                    <td style=\"\">MCOLN1<\/td>\n                    <td style=\"\">Mukopolysaccharidose Typ 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.743,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_639\">\n                    <td style=\"\">MECP2<\/td>\n                    <td style=\"\">neonatale schwere Mikrozephalie mit Enzephalopathy<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.497,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_640\">\n                    <td style=\"\">MECP2<\/td>\n                    <td style=\"\">Rett-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.497,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_641\">\n                    <td style=\"\">MECP2<\/td>\n                    <td style=\"\">Xq28-Duplikation-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.497,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_642\">\n                    <td style=\"\">MED13L<\/td>\n                    <td style=\"\">Kongenitale unkorrigierte Transposition der gro\u00dfen Arterien<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.669,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_643\">\n                    <td style=\"\">MED17<\/td>\n                    <td style=\"\">Infantile zerebrale und zerebell\u00e4re Atrophie mit postnataler progressive Mikrozephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.956,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_644\">\n                    <td style=\"\">MEF2C<\/td>\n                    <td style=\"\">Mikrodeletionssyndrom 5q14.3<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.452,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_645\">\n                    <td style=\"\">MEFV - HS1<\/td>\n                    <td style=\"\">FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL RECESSIVE<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.766,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_646\">\n                    <td style=\"\">MEFV - HS1<\/td>\n                    <td style=\"\">FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.766,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_647\">\n                    <td style=\"\">MEFV - HS2<\/td>\n                    <td style=\"\">FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.568,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_648\">\n                    <td style=\"\">MEFV - HS2<\/td>\n                    <td style=\"\">FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL RECESSIVE<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.568,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_649\">\n                    <td style=\"\">MEFV - HS3<\/td>\n                    <td style=\"\">FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL RECESSIVE<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">776,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_650\">\n                    <td style=\"\">MEFV - HS3<\/td>\n                    <td style=\"\">FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">776,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_651\">\n                    <td style=\"\">MEN1<\/td>\n                    <td style=\"\">endokrine multiple Neoplasie Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.959,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_652\">\n                    <td style=\"\">MEN1<\/td>\n                    <td style=\"\">famili\u00e4r isolierter Hyperparathyreoidismus (FIHPT)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.959,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_653\">\n                    <td style=\"\">MEOX1<\/td>\n                    <td style=\"\">Klippel-Feil-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">765,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_654\">\n                    <td style=\"\">MFN2<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit Typ 2A2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.427,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_655\">\n                    <td style=\"\">MFSD8<\/td>\n                    <td style=\"\">Neuronale Ceroid-Lipofuszinose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.557,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_656\">\n                    <td style=\"\">MFSD8<\/td>\n                    <td style=\"\">progressive Epilepsie mit Intelligenzminderung, Finnischer Typ<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.557,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_657\">\n                    <td style=\"\">MGAT2<\/td>\n                    <td style=\"\">CDG-Syndrom 2a<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.344,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_658\">\n                    <td style=\"\">MGME1<\/td>\n                    <td style=\"\">Mitochondriales DNA-Depletionssyndrom, 11<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.035,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_659\">\n                    <td style=\"\">MID1<\/td>\n                    <td style=\"\">Opitz GBBB Syndrom 1 (X-linked)<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.004,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_660\">\n                    <td style=\"\">MITF<\/td>\n                    <td style=\"\">Waardenburg-Syndrom Typ 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.581,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_661\">\n                    <td style=\"\">MITF<\/td>\n                    <td style=\"\">Tietz-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.581,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_662\">\n                    <td style=\"\">MOCS1<\/td>\n                    <td style=\"\">Sulfitoxidase-Mangel durch Molybd\u00e4n-Cofaktor-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.911,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_663\">\n                    <td style=\"\">MPDZ<\/td>\n                    <td style=\"\">Hydrozephalus, kommunizierender, kongenitaler<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.213,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_664\">\n                    <td style=\"\">MPI<\/td>\n                    <td style=\"\">CDG-Syndrom Typ Ib<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.272,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_665\">\n                    <td style=\"\">MPL<\/td>\n                    <td style=\"\">Thrombozyth\u00e4mie 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.908,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_666\">\n                    <td style=\"\">MPL<\/td>\n                    <td style=\"\">Amegakaryozytische Thrombozytopenie, kongenitale<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.908,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_667\">\n                    <td style=\"\">MPL<\/td>\n                    <td style=\"\">Myelofibrose mit myeloider Metaplasie, somatisch<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.908,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_668\">\n                    <td style=\"\">MPZ<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit Typ 2J<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">939,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_669\">\n                    <td style=\"\">MPZ<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit Typ 2I<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">939,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_670\">\n                    <td style=\"\">MRE11<\/td>\n                    <td style=\"\">Ataxia teleangiectatica (AT)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.127,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_671\">\n                    <td style=\"\">MRE11<\/td>\n                    <td style=\"\">Ataxia teleangiectatica (AT)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.127,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_672\">\n                    <td style=\"\">MSH3<\/td>\n                    <td style=\"\">Kolon-Karzinom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.414,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_673\">\n                    <td style=\"\">MSX1<\/td>\n                    <td style=\"\">Witkop Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">912,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_674\">\n                    <td style=\"\">MSX1<\/td>\n                    <td style=\"\">Oligodontie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">912,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_675\">\n                    <td style=\"\">MSX1<\/td>\n                    <td style=\"\">Orofaciale Spaltbildung Typ 5<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">912,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_676\">\n                    <td style=\"\">mtDNA<\/td>\n                    <td style=\"\">Mitochondriopathien<\/td>\n                    <td style=\"\">Sequenzierung der gesamten DNA<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">16.569,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_677\">\n                    <td style=\"\">MTM1<\/td>\n                    <td style=\"\">X-chromosomale zentronukle\u00e4re Myopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.857,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_678\">\n                    <td style=\"\">MT-ND4<\/td>\n                    <td style=\"\">Lebersche Optikusatrophie (LHON)<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.378,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_679\">\n                    <td style=\"\">MTRFR<\/td>\n                    <td style=\"\">Kombinierter Defekt der oxidativen Phosphorylierung Typ 7<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">501,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_680\">\n                    <td style=\"\">MTTP<\/td>\n                    <td style=\"\">Abetalipoprotein\u00e4mie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.685,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_681\">\n                    <td style=\"\">MUSK<\/td>\n                    <td style=\"\">MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.610,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_682\">\n                    <td style=\"\">MUSK<\/td>\n                    <td style=\"\">FETAL AKINESIA DEFORMATION SEQUENCE; FADS<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.610,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_683\">\n                    <td style=\"\">MUTYH<\/td>\n                    <td style=\"\">adenomat\u00f6se attenuierte famili\u00e4re Polyposis<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.650,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_684\">\n                    <td style=\"\">MVK<\/td>\n                    <td style=\"\">Hyper-IgD Syndrom<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.191,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_685\">\n                    <td style=\"\">MVK<\/td>\n                    <td style=\"\">Porokeratose, aktinische disseminierte superfizielle<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.191,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_686\">\n                    <td style=\"\">MVK<\/td>\n                    <td style=\"\">Mevalon-Azidurie<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.191,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_687\">\n                    <td style=\"\">MYBPC3<\/td>\n                    <td style=\"\">Kardiomyopathie, dilatative  (DCM)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.825,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_688\">\n                    <td style=\"\">MYCN<\/td>\n                    <td style=\"\">Feingold-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.395,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_689\">\n                    <td style=\"\">MYD88<\/td>\n                    <td style=\"\">MYD88 Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">915,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_690\">\n                    <td style=\"\">MYH11<\/td>\n                    <td style=\"\">Famili\u00e4res thorakales Aortenaneurysma und Aortendissektion Typ 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.940,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_691\">\n                    <td style=\"\">MYH3<\/td>\n                    <td style=\"\">Arthrogrypose, distal, Typ 2B<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.823,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_692\">\n                    <td style=\"\">MYH3<\/td>\n                    <td style=\"\">Freeman-Sheldon-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.823,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_693\">\n                    <td style=\"\">MYH3<\/td>\n                    <td style=\"\">Dysmorphien, digitotalare<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.823,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_694\">\n                    <td style=\"\">MYH7<\/td>\n                    <td style=\"\">Linksventrikul\u00e4re Noncompaction-Kardiomyopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.835,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_695\">\n                    <td style=\"\">MYH7<\/td>\n                    <td style=\"\">Kardiomyopathie, dilatative  (DCM)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.835,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_696\">\n                    <td style=\"\">MYH7<\/td>\n                    <td style=\"\">Myopathie, distale, Typ Laing<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.835,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_697\">\n                    <td style=\"\">MYH9<\/td>\n                    <td style=\"\">May-Hegglin Anomalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.946,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_698\">\n                    <td style=\"\">MYH9<\/td>\n                    <td style=\"\">Epstein Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.946,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_699\">\n                    <td style=\"\">MYH9<\/td>\n                    <td style=\"\">Makrothrombozytopenie und progressive sensorineurale Taubheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.946,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_700\">\n                    <td style=\"\">MYH9<\/td>\n                    <td style=\"\">Fechtner Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.946,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_701\">\n                    <td style=\"\">MYH9<\/td>\n                    <td style=\"\">Schwerh\u00f6rigkeit, autosomal dominant<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.946,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_702\">\n                    <td style=\"\">MYH9<\/td>\n                    <td style=\"\">Sebastian Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.946,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_703\">\n                    <td style=\"\">MYMK<\/td>\n                    <td style=\"\">Carey-Fineman-Ziter Syndrome<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">666,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_704\">\n                    <td style=\"\">NAGLU<\/td>\n                    <td style=\"\">MucopolysaccharidoseTyp IIIB (Sanfilippo B)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.232,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_705\">\n                    <td style=\"\">NAGLU<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit Typ 2V<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.232,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_706\">\n                    <td style=\"\">NDE1<\/td>\n                    <td style=\"\">Mikrohydranenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.008,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_707\">\n                    <td style=\"\">NDE1<\/td>\n                    <td style=\"\">Lissenzephalie 4 (mit Mikrozephalie)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.008,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_708\">\n                    <td style=\"\">NDP<\/td>\n                    <td style=\"\">Retinopathie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">402,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_709\">\n                    <td style=\"\">NELFA<\/td>\n                    <td style=\"\">Wolf-Hirschhorn Syndrome<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.620,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_710\">\n                    <td style=\"\">NF1<\/td>\n                    <td style=\"\">Watson-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.550,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_711\">\n                    <td style=\"\">NF1<\/td>\n                    <td style=\"\">Noonan-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.550,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_712\">\n                    <td style=\"\">NF1<\/td>\n                    <td style=\"\">Famili\u00e4re segmentale  Neurofibromatose 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.550,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_713\">\n                    <td style=\"\">NF1<\/td>\n                    <td style=\"\">Neurofibromatose 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.550,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_714\">\n                    <td style=\"\">NF2<\/td>\n                    <td style=\"\">Neurofibromatose 2<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.788,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_715\">\n                    <td style=\"\">NFIX<\/td>\n                    <td style=\"\">Marshall-Smith-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.533,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_716\">\n                    <td style=\"\">NFIX<\/td>\n                    <td style=\"\">Sotos Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.533,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_717\">\n                    <td style=\"\">NGF<\/td>\n                    <td style=\"\">Heredit\u00e4re sensible und autonome Neuropathie Typ 5 (HSAN5)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">726,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_718\">\n                    <td style=\"\">NHEJ1<\/td>\n                    <td style=\"\">kombinierter schwerer Immundefekt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">915,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_719\">\n                    <td style=\"\">NHLRC1<\/td>\n                    <td style=\"\">Lafora Krankheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.188,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_720\">\n                    <td style=\"\">NIPBL<\/td>\n                    <td style=\"\">Cornelia de Lange Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.415,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_721\">\n                    <td style=\"\">NKX2-1<\/td>\n                    <td style=\"\">Benign Chorea<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.206,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_722\">\n                    <td style=\"\">NKX2-5<\/td>\n                    <td style=\"\">Schilddr\u00fcsenhypoplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">975,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_723\">\n                    <td style=\"\">NLGN3<\/td>\n                    <td style=\"\">Asperger Syndrom Pr\u00e4disposition X-gekoppelt 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.547,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_724\">\n                    <td style=\"\">NLGN3<\/td>\n                    <td style=\"\">Autismus Pr\u00e4disposition X-gekoppelt 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.547,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_725\">\n                    <td style=\"\">NLGN4X<\/td>\n                    <td style=\"\">Asperger Syndrom Pr\u00e4disposition X-gekoppelt 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.511,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_726\">\n                    <td style=\"\">NLGN4X<\/td>\n                    <td style=\"\">Mentale Retardierung, x-gekoppelt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.511,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_727\">\n                    <td style=\"\">NLGN4X<\/td>\n                    <td style=\"\">Autismus Pr\u00e4disposition X-gekoppelt 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.511,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_728\">\n                    <td style=\"\">NLRC4<\/td>\n                    <td style=\"\">K\u00e4lte-Urtikaria, famili\u00e4re<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.075,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_729\">\n                    <td style=\"\">NLRC4<\/td>\n                    <td style=\"\">Periodisches Fieber-infantile Enterocolitis-autoinflammatorisches Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.075,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_730\">\n                    <td style=\"\">NLRP3<\/td>\n                    <td style=\"\">Muckle-Wells-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.111,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_731\">\n                    <td style=\"\">NLRP3<\/td>\n                    <td style=\"\">Famili\u00e4res autoinflammatorisches K\u00e4ltesyndrom (FCAS)<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.111,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_732\">\n                    <td style=\"\">NLRP3<\/td>\n                    <td style=\"\">Chronisch-infantiles neuro-kutaneo-artikul\u00e4res (CINCA) Syndrom<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.111,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_733\">\n                    <td style=\"\">NME8<\/td>\n                    <td style=\"\">Prim\u00e4re zili\u00e4re Dyskinesie, 6<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.767,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_734\">\n                    <td style=\"\">NOD2<\/td>\n                    <td style=\"\">M. Crohn (drei h\u00e4ufigste pr\u00e4disponierende Mutationen des NOD2-Gens)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.123,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_735\">\n                    <td style=\"\">NOD2<\/td>\n                    <td style=\"\">Blau-Syndrom\/\u201cearly-onset\u201c-Sarkoidose (Mutation in Exon 4 des NOD2-Gens)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.123,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_736\">\n                    <td style=\"\">NOL3<\/td>\n                    <td style=\"\">Myoklonie, famili\u00e4r, kortikal<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">660,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_737\">\n                    <td style=\"\">NOTCH3<\/td>\n                    <td style=\"\">CADASIL<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.966,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_738\">\n                    <td style=\"\">NPC1<\/td>\n                    <td style=\"\">Niemann Pick Erkrankung Typ C<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.837,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_739\">\n                    <td style=\"\">NPC2<\/td>\n                    <td style=\"\">Niemann Pick Erkrankung Typ C<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">525,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_740\">\n                    <td style=\"\">NPHP1<\/td>\n                    <td style=\"\">Joubert Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.202,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_741\">\n                    <td style=\"\">NPHP1<\/td>\n                    <td style=\"\">Senior-Loken Syndrom 1<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.202,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_742\">\n                    <td style=\"\">NPHP3<\/td>\n                    <td style=\"\">Meckel Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.993,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_743\">\n                    <td style=\"\">NPHP4<\/td>\n                    <td style=\"\">Senior-Loken Syndrom 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.281,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_744\">\n                    <td style=\"\">NR2E3<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.233,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_745\">\n                    <td style=\"\">NR2E3<\/td>\n                    <td style=\"\">Goldmann-Favre-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.233,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_746\">\n                    <td style=\"\">NR5A1<\/td>\n                    <td style=\"\">St\u00f6rung dere Geschlechtsentwicklung 46,XX, ovotestikul\u00e4re<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.386,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_747\">\n                    <td style=\"\">NR5A1<\/td>\n                    <td style=\"\">46, XX testikul\u00e4re St\u00f6rung des Geschlechtsentwicklung<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.386,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_748\">\n                    <td style=\"\">NR5A1<\/td>\n                    <td style=\"\">m\u00e4nnliche Infertilit\u00e4t mit Azoospermie oder Oligozoospermie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.386,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_749\">\n                    <td style=\"\">NR5A1<\/td>\n                    <td style=\"\">Gonadendysgenesie, 46, XX-Typ<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.386,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_750\">\n                    <td style=\"\">NR5A1<\/td>\n                    <td style=\"\">46, XY - Gonadendysgenesie, partielle und vollst\u00e4ndige<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.386,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_751\">\n                    <td style=\"\">NRXN1<\/td>\n                    <td style=\"\">Pitt-Hopkins-\u00e4hnliches Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.644,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_752\">\n                    <td style=\"\">NSD1<\/td>\n                    <td style=\"\">Sotos Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.091,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_753\">\n                    <td style=\"\">NSD1<\/td>\n                    <td style=\"\">Weaver Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.091,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_754\">\n                    <td style=\"\">NSD2<\/td>\n                    <td style=\"\">Wolf-Hirschhorn Syndrome<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.098,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_755\">\n                    <td style=\"\">NTNG1<\/td>\n                    <td style=\"\">Atypisches Rett-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.620,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_756\">\n                    <td style=\"\">NYX<\/td>\n                    <td style=\"\">Kongenitale station\u00e4re Nachtblindheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.431,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_757\">\n                    <td style=\"\">OAT<\/td>\n                    <td style=\"\">Atrophia gyrata der Chorioidea und Retina<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.320,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_758\">\n                    <td style=\"\">OCA2<\/td>\n                    <td style=\"\">Albinismus, okulokutaner, Typ II<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.517,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_759\">\n                    <td style=\"\">OCA2<\/td>\n                    <td style=\"\">Albinismus, braun okulokutan<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.517,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_760\">\n                    <td style=\"\">OCRL<\/td>\n                    <td style=\"\">Dent-Krankheit Typ 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.706,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_761\">\n                    <td style=\"\">OCRL<\/td>\n                    <td style=\"\">Lowe Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.706,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_762\">\n                    <td style=\"\">OFD1<\/td>\n                    <td style=\"\">Oro-fazio-digitales Syndrom Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.039,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_763\">\n                    <td style=\"\">OFD1<\/td>\n                    <td style=\"\">Joubert Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.039,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_764\">\n                    <td style=\"\">OFD1<\/td>\n                    <td style=\"\">Simpson-Golabi-Behmel-Syndrom Typ 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.039,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_765\">\n                    <td style=\"\">OGDH<\/td>\n                    <td style=\"\">Oxoglutarazidurie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.105,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_766\">\n                    <td style=\"\">OPA1<\/td>\n                    <td style=\"\">Optikusatrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.048,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_767\">\n                    <td style=\"\">OPA3<\/td>\n                    <td style=\"\">Optikusatrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">543,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_768\">\n                    <td style=\"\">OPHN1<\/td>\n                    <td style=\"\">X-chromosomale geistige Retardierung - zerebell\u00e4re Hypoplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.409,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_769\">\n                    <td style=\"\">OPTN<\/td>\n                    <td style=\"\">Kongenitales Glaukom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.734,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_770\">\n                    <td style=\"\">ORAI1<\/td>\n                    <td style=\"\">Myopathie, tubular, aggregat, 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">912,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_771\">\n                    <td style=\"\">ORAI1<\/td>\n                    <td style=\"\">Immundefizienz 9<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">912,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_772\">\n                    <td style=\"\">ORC4<\/td>\n                    <td style=\"\">Meier-Gorlin Syndrom 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.311,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_773\">\n                    <td style=\"\">ORC6<\/td>\n                    <td style=\"\">Meier-Gorlin Syndrom 3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">759,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_774\">\n                    <td style=\"\">OTOF<\/td>\n                    <td style=\"\">Autosomal-rezessive nicht-syndromale sensorineurale Schwerh\u00f6rigkeit Typ DFNB<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.994,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_775\">\n                    <td style=\"\">OTX2<\/td>\n                    <td style=\"\">Syndromale Mikrophthalmie Typ 5<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">894,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_776\">\n                    <td style=\"\">OTX2<\/td>\n                    <td style=\"\">Fr\u00fchzeitige Retinale Dystrophie und Hypophysenfehlfunktion<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">894,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_777\">\n                    <td style=\"\">P2RX7<\/td>\n                    <td style=\"\">Chronische lymphatische Leuk\u00e4mie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.788,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_778\">\n                    <td style=\"\">PABPN1<\/td>\n                    <td style=\"\">Okulo-pharyngeale Muskeldystrophie (OPMD)<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">921,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_779\">\n                    <td style=\"\">PAFAH1B1<\/td>\n                    <td style=\"\">Lissenzephalie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.287,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_780\">\n                    <td style=\"\">PAH<\/td>\n                    <td style=\"\">Phenylketonurie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.359,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_781\">\n                    <td style=\"\">PALB2<\/td>\n                    <td style=\"\">heredit\u00e4rer Brustkrebs<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.567,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_782\">\n                    <td style=\"\">PANK2<\/td>\n                    <td style=\"\">Neurodegeneration mit Eisenablagerung im Gehirn (NBIA)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.713,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_783\">\n                    <td style=\"\">PARK7<\/td>\n                    <td style=\"\">Juveniles Parkinson-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">570,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_784\">\n                    <td style=\"\">PAX6<\/td>\n                    <td style=\"\">Katarakt mit sp\u00e4t einsetzender kornealer Dystrophie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.467,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_785\">\n                    <td style=\"\">PAX6<\/td>\n                    <td style=\"\">Aniridie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.467,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_786\">\n                    <td style=\"\">PAX6<\/td>\n                    <td style=\"\">Sehnerv-Hypoplasie, isolierte<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.467,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_787\">\n                    <td style=\"\">PAX6<\/td>\n                    <td style=\"\">Kolomba, okular<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.467,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_788\">\n                    <td style=\"\">PAX8<\/td>\n                    <td style=\"\">Schilddr\u00fcsenhypoplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.362,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_789\">\n                    <td style=\"\">PCDH19<\/td>\n                    <td style=\"\">Epileptische Enzephalopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.447,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_790\">\n                    <td style=\"\">PDE4D<\/td>\n                    <td style=\"\">Akrodysostose 2, mit oder ohne Hormonresistenz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.430,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_791\">\n                    <td style=\"\">PDE6C<\/td>\n                    <td style=\"\">Achromatopsie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.577,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_792\">\n                    <td style=\"\">PDE6H<\/td>\n                    <td style=\"\">Zapfen-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">252,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_793\">\n                    <td style=\"\">PDHA1<\/td>\n                    <td style=\"\">Pyruvat Dehydrogenase (PDH) Defizienz<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.287,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_794\">\n                    <td style=\"\">PEX1<\/td>\n                    <td style=\"\">Zellweger Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.852,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_795\">\n                    <td style=\"\">PEX1<\/td>\n                    <td style=\"\">Refsum-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.852,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_796\">\n                    <td style=\"\">PEX10<\/td>\n                    <td style=\"\">Zellweger Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_797\">\n                    <td style=\"\">PEX12<\/td>\n                    <td style=\"\">Zellweger Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.080,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_798\">\n                    <td style=\"\">PEX2<\/td>\n                    <td style=\"\">Zellweger Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">918,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_799\">\n                    <td style=\"\">PEX26<\/td>\n                    <td style=\"\">Zellweger Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">918,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_800\">\n                    <td style=\"\">PEX5<\/td>\n                    <td style=\"\">Zellweger Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.965,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_801\">\n                    <td style=\"\">PEX6<\/td>\n                    <td style=\"\">Zellweger Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.943,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_802\">\n                    <td style=\"\">PEX7<\/td>\n                    <td style=\"\">Refsum-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">972,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_803\">\n                    <td style=\"\">PFN1<\/td>\n                    <td style=\"\">Amyotrophe Lateralsklerose (ALS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">423,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_804\">\n                    <td style=\"\">PGAM2<\/td>\n                    <td style=\"\">Glykogenspeichererkrankung X<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">762,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_805\">\n                    <td style=\"\">PGK1<\/td>\n                    <td style=\"\">Phosphoglyceratkinase 1 Defizienz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.254,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_806\">\n                    <td style=\"\">PHEX<\/td>\n                    <td style=\"\">Hypophosphat\u00e4mische Rachitis, x-gekoppelt, dominant<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.250,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_807\">\n                    <td style=\"\">PHF6<\/td>\n                    <td style=\"\">B\u00f6rjeson-Forssman-Lehmann-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.098,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_808\">\n                    <td style=\"\">PHYH<\/td>\n                    <td style=\"\">Refsum Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.017,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_809\">\n                    <td style=\"\">PIGA<\/td>\n                    <td style=\"\">Paroxysomale n\u00e4chtliche H\u00e4moglobinurie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.455,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_810\">\n                    <td style=\"\">PIK3R2<\/td>\n                    <td style=\"\">Megalenzephalie - Polymikrogyrie - postaxiale Polydaktylie - Hydrozephalus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.187,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_811\">\n                    <td style=\"\">PINK1<\/td>\n                    <td style=\"\">Juveniles Parkinson-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.746,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_812\">\n                    <td style=\"\">PITX2<\/td>\n                    <td style=\"\">Rieger-Axenfeld-Anomalie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">975,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_813\">\n                    <td style=\"\">PITX2<\/td>\n                    <td style=\"\">Peters-Anomalie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">975,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_814\">\n                    <td style=\"\">PKD1<\/td>\n                    <td style=\"\">autosomal-dominante polyzystische  Nierenerkrankung, Typ 1  (ADPKD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">12.912,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_815\">\n                    <td style=\"\">PKD2<\/td>\n                    <td style=\"\">Autosomal-dominante polyzystische Nierenerkrankung, Typ 2 (ADPKD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.907,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_816\">\n                    <td style=\"\">PKHD1<\/td>\n                    <td style=\"\">Autosomal-rezessive polyzystische Nierenerkrankung (ARPKD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">12.225,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_817\">\n                    <td style=\"\">PKLR<\/td>\n                    <td style=\"\">Pyruvatkinase-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.725,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_818\">\n                    <td style=\"\">PLA2G5<\/td>\n                    <td style=\"\">Benigne-famili\u00e4re, gefleckte Retina<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">417,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_819\">\n                    <td style=\"\">PLA2G6<\/td>\n                    <td style=\"\">Parkinsonismus und Dystonie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.463,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_820\">\n                    <td style=\"\">PLA2G6<\/td>\n                    <td style=\"\">Neurodegeneration mit Eisenablagerung im Gehirn (NBIA)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.463,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_821\">\n                    <td style=\"\">PLCB1<\/td>\n                    <td style=\"\">fr\u00fchinfantile epileptische Enzephalopathie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.651,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_822\">\n                    <td style=\"\">PLCB1<\/td>\n                    <td style=\"\">fr\u00fchinfantile epileptische Enzephalopathie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.651,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_823\">\n                    <td style=\"\">PLCG2<\/td>\n                    <td style=\"\">Familial Cold Autoinflammatory Syndrom 3<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.798,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_824\">\n                    <td style=\"\">PLCG2<\/td>\n                    <td style=\"\">Autoinflammation, Antik\u00f6rperdefizienz und Immundysregulation-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.798,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_825\">\n                    <td style=\"\">PLEC<\/td>\n                    <td style=\"\">Muskeldystrophie, Gliederg\u00fcrtel, Typ 2Q<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">14.055,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_826\">\n                    <td style=\"\">PLEC<\/td>\n                    <td style=\"\">Epidermolysis bullosa simplex, mit Muskeldystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">14.055,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_827\">\n                    <td style=\"\">PLEC<\/td>\n                    <td style=\"\">Epidermolysis bullosa simplex, mit Nageldystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">14.055,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_828\">\n                    <td style=\"\">PLEC<\/td>\n                    <td style=\"\">Epidermolysis bullosa simplex, mit Pylorusatresie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">14.055,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_829\">\n                    <td style=\"\">PLEC<\/td>\n                    <td style=\"\">Epidermolysis bullosa simplex, Ogna-Typ<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">14.055,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_830\">\n                    <td style=\"\">PLP1<\/td>\n                    <td style=\"\">Spastische Paraplegie 2, X-gekoppelt<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">834,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_831\">\n                    <td style=\"\">PLP1<\/td>\n                    <td style=\"\">Pelizaeus-Merzbacher-Krankheit<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">834,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_832\">\n                    <td style=\"\">PMM2<\/td>\n                    <td style=\"\">CDG-Syndrom 1a<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">741,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_833\">\n                    <td style=\"\">PMP22<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit Typ 1A<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">654,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_834\">\n                    <td style=\"\">PMP22<\/td>\n                    <td style=\"\">Heredit\u00e4re Neuropathie mit Neigung zu Druckparesen<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">654,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_835\">\n                    <td style=\"\">PNKD<\/td>\n                    <td style=\"\">Paroxysmale Nonkinesiogene Dyskinesie 1 PNKD1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.275,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_836\">\n                    <td style=\"\">PNKP<\/td>\n                    <td style=\"\">Mikrozephalie-Kr\u00e4mpfe-Entwicklungsverz\u00f6gerung-Syndrom (MCSZ)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.566,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_837\">\n                    <td style=\"\">PNPLA3<\/td>\n                    <td style=\"\">Pr\u00e4disposition f\u00fcr nichtalkoholische Fettleber-Erkrankung (PNPLA3-Gen)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.446,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_838\">\n                    <td style=\"\">PNPO<\/td>\n                    <td style=\"\">Pyridoxamine 5-prime-phosphate oxidase deficiency<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">786,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_839\">\n                    <td style=\"\">POLE<\/td>\n                    <td style=\"\">FILS-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.861,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_840\">\n                    <td style=\"\">POLG<\/td>\n                    <td style=\"\">Mitochondriales rezessives Ataxie Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.720,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_841\">\n                    <td style=\"\">POLG<\/td>\n                    <td style=\"\">Externe progressive Ophthalmoplegie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.720,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_842\">\n                    <td style=\"\">POLG<\/td>\n                    <td style=\"\">POLG-Related Ataxia Neuropathy Spectrum Disorders<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.720,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_843\">\n                    <td style=\"\">POLG<\/td>\n                    <td style=\"\">Alpers Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.720,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_844\">\n                    <td style=\"\">POLG2<\/td>\n                    <td style=\"\">Externe progressive Ophthalmoplegie Typ 1 (PEOA1)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.458,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_845\">\n                    <td style=\"\">POLR1C<\/td>\n                    <td style=\"\">Treacher Collins Syndrom 3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_846\">\n                    <td style=\"\">POLR1C<\/td>\n                    <td style=\"\">Leukodystrophie, hypomyelisierend, Typ 11<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_847\">\n                    <td style=\"\">POLR1D<\/td>\n                    <td style=\"\">Treacher Collins Syndrom 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">402,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_848\">\n                    <td style=\"\">POLR3A<\/td>\n                    <td style=\"\">4-H-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.173,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_849\">\n                    <td style=\"\">POU1F1<\/td>\n                    <td style=\"\">Hypophysale Hormondefizienz, kombiniert 1<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">954,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_850\">\n                    <td style=\"\">PPM1K<\/td>\n                    <td style=\"\">Ahornsirup-Krankheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.119,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_851\">\n                    <td style=\"\">PPT1<\/td>\n                    <td style=\"\">Neuronale Ceroid-Lipofuszinose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.008,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_852\">\n                    <td style=\"\">PQBP1<\/td>\n                    <td style=\"\">Renpenning-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">798,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_853\">\n                    <td style=\"\">PRF1<\/td>\n                    <td style=\"\">Lymphohistiozytose, h\u00e4mophagozytische, famili\u00e4re Form 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.668,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_854\">\n                    <td style=\"\">PRF1<\/td>\n                    <td style=\"\">Lymphom, Non-Hodgkin<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.668,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_855\">\n                    <td style=\"\">PRICKLE1<\/td>\n                    <td style=\"\">Unverricht-Lundborg-Krankheit (ULD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.496,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_856\">\n                    <td style=\"\">PRICKLE1<\/td>\n                    <td style=\"\">Progressive Myoclonus Epilepsie mit Ataxie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.496,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_857\">\n                    <td style=\"\">PRKAR1A<\/td>\n                    <td style=\"\">Carney-Komplex<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.146,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_858\">\n                    <td style=\"\">PRKCG<\/td>\n                    <td style=\"\">Spinocerebellare Ataxie 14<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.133,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_859\">\n                    <td style=\"\">PRKN<\/td>\n                    <td style=\"\">Juveniles Parkinson-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.398,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_860\">\n                    <td style=\"\">PRKRA<\/td>\n                    <td style=\"\">Dystonie, DYT16<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">942,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_861\">\n                    <td style=\"\">PRKRA<\/td>\n                    <td style=\"\">Early Onset Dystonie mit Parkinsonismus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">942,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_862\">\n                    <td style=\"\">PRNP<\/td>\n                    <td style=\"\">Creutzfeldt-Jakob-Krankheit (CJD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">762,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_863\">\n                    <td style=\"\">PROC<\/td>\n                    <td style=\"\">THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL DOMINANT; THPH3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.488,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_864\">\n                    <td style=\"\">PROM1<\/td>\n                    <td style=\"\">Zapfen-St\u00e4bchen-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.598,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_865\">\n                    <td style=\"\">PROP1<\/td>\n                    <td style=\"\">Hypophysale Hormondefizienz, kombiniert 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">681,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_866\">\n                    <td style=\"\">PRPF31<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.500,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_867\">\n                    <td style=\"\">PRPH2<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_868\">\n                    <td style=\"\">PRPH2<\/td>\n                    <td style=\"\">Macula-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_869\">\n                    <td style=\"\">PRPH2<\/td>\n                    <td style=\"\">Aderhaut-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_870\">\n                    <td style=\"\">PRPH2<\/td>\n                    <td style=\"\">Zapfen-St\u00e4bchen-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.041,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_871\">\n                    <td style=\"\">PRPS1<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth-Krankheit, X-chromosomale, Typ 5<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">966,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_872\">\n                    <td style=\"\">PRPS1<\/td>\n                    <td style=\"\">nicht-syndromale sensorineurale X-chromosomale Schwerh\u00f6rigkeit, Typ DFN<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">966,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_873\">\n                    <td style=\"\">PRRT2<\/td>\n                    <td style=\"\">Epilepsie, benigne famili\u00e4re infantile (BFIE)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.185,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_874\">\n                    <td style=\"\">PRRT2<\/td>\n                    <td style=\"\">Infantile Konvulsion und Coreoatheose<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.185,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_875\">\n                    <td style=\"\">PRRT2<\/td>\n                    <td style=\"\">Famili\u00e4re paroxysmale kinesiogene Dyskinesie (PKD)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.185,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_876\">\n                    <td style=\"\">PRSS1<\/td>\n                    <td style=\"\">Trypsinogen-Defizienz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">744,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_877\">\n                    <td style=\"\">PRSS1<\/td>\n                    <td style=\"\">Pankreatitis, erblich<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">744,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_878\">\n                    <td style=\"\">PSAP<\/td>\n                    <td style=\"\">Gaucher-Krankheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.575,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_879\">\n                    <td style=\"\">PSAP<\/td>\n                    <td style=\"\">Metachromatische Leukodystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.575,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_880\">\n                    <td style=\"\">PSAP<\/td>\n                    <td style=\"\">Enzephalopathie durch Prosaposin-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.575,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_881\">\n                    <td style=\"\">PSEN1<\/td>\n                    <td style=\"\">Alzheimer Demenz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.431,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_882\">\n                    <td style=\"\">PSEN2<\/td>\n                    <td style=\"\">Alzheimer Demenz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.584,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_883\">\n                    <td style=\"\">PSMB8<\/td>\n                    <td style=\"\">Autoinflammation, Lipodystrophie und Dermatose (ALDD)-Syndrom (auch Nakajo-Nishimura- oder CANDLE-Syndrom; PSMB8-Gen)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">831,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_884\">\n                    <td style=\"\">PSTPIP1<\/td>\n                    <td style=\"\">PAPA-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.446,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_885\">\n                    <td style=\"\">PTCH1<\/td>\n                    <td style=\"\">Holoprosenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.344,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_886\">\n                    <td style=\"\">PTCH2<\/td>\n                    <td style=\"\">Basalzelln\u00e4vus \/ Gorlin-Sydrom \/ Gorlin-Goltz-Syndrom \/ N\u00e4voides Basalzellkarzinom-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.612,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_887\">\n                    <td style=\"\">PTCH2<\/td>\n                    <td style=\"\">Medullablastom, desmoplastisch<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.612,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_888\">\n                    <td style=\"\">PTCH2<\/td>\n                    <td style=\"\">somatisches Basalzellenkarzinom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.612,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_889\">\n                    <td style=\"\">PTDSS1<\/td>\n                    <td style=\"\">Hyperostoischer Kleinwuchs Typ Lenz-Majewski<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.422,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_890\">\n                    <td style=\"\">PTEN<\/td>\n                    <td style=\"\">Bannayan-Riley-Ruvalcaba-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.731,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_891\">\n                    <td style=\"\">PTEN<\/td>\n                    <td style=\"\">Lhermitte-Duclos-Krankheit<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.731,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_892\">\n                    <td style=\"\">PTEN<\/td>\n                    <td style=\"\">Cowden-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.731,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_893\">\n                    <td style=\"\">PTEN<\/td>\n                    <td style=\"\">Makrozephalie-Autismus-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.731,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_894\">\n                    <td style=\"\">PTH<\/td>\n                    <td style=\"\">HYPOPARATHYROIDISM, AUTOSOMAL RECESSIVE<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">348,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_895\">\n                    <td style=\"\">PTH<\/td>\n                    <td style=\"\">HYPOPARATHYROIDISM, AUTOSOMAL DOMINANT<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">348,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_896\">\n                    <td style=\"\">PTPN11<\/td>\n                    <td style=\"\">LEOPARD-Sydrom 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.016,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_897\">\n                    <td style=\"\">PTPN11<\/td>\n                    <td style=\"\">Noonan-Syndrom 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.016,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_898\">\n                    <td style=\"\">PTPN11<\/td>\n                    <td style=\"\">Metachondromatose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.016,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_899\">\n                    <td style=\"\">PTPN11<\/td>\n                    <td style=\"\">Juvenile myelomonzyt\u00e4re Leuk\u00e4mie, somatisch<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.016,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_900\">\n                    <td style=\"\">PTS<\/td>\n                    <td style=\"\">6-Pyruvoyl-Tetrahydropterin-Synthase-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">438,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_901\">\n                    <td style=\"\">PYGM<\/td>\n                    <td style=\"\">Glykogen-Speicherkrankheit Typ 5<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.529,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_902\">\n                    <td style=\"\">QDPR<\/td>\n                    <td style=\"\">Dihydropteridinreduktase-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">735,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_903\">\n                    <td style=\"\">RAB3GAP1<\/td>\n                    <td style=\"\">Warburg Mikro-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.967,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_904\">\n                    <td style=\"\">RAD21<\/td>\n                    <td style=\"\">Cornelia de Lange Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.896,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_905\">\n                    <td style=\"\">RAD51<\/td>\n                    <td style=\"\">Spiegelbewegungen, famili\u00e4re kongenitale, 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.023,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_906\">\n                    <td style=\"\">RAD51D<\/td>\n                    <td style=\"\">Heredit\u00e4res Brust- und Ovarialkrebssyndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.047,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_907\">\n                    <td style=\"\">RAI1<\/td>\n                    <td style=\"\">Smith-Magenis Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.721,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_908\">\n                    <td style=\"\">RAPSN<\/td>\n                    <td style=\"\">Myasthenes Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.239,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_909\">\n                    <td style=\"\">RARS2<\/td>\n                    <td style=\"\">pontozerebell\u00e4re Hypoplasie Typ 6<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.827,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_910\">\n                    <td style=\"\">RBBP8<\/td>\n                    <td style=\"\">Jawad Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.709,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_911\">\n                    <td style=\"\">RBBP8<\/td>\n                    <td style=\"\">Seckel Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.709,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_912\">\n                    <td style=\"\">RBM10<\/td>\n                    <td style=\"\">TARP-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.988,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_913\">\n                    <td style=\"\">RBP3<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.744,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_914\">\n                    <td style=\"\">REEP1<\/td>\n                    <td style=\"\">Spastische Paraplegie Typ 31<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">855,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_915\">\n                    <td style=\"\">REPS1<\/td>\n                    <td style=\"\">Neurodegeneration mit Eisenablagerung im Gehirn (NBIA)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.391,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_916\">\n                    <td style=\"\">RHO<\/td>\n                    <td style=\"\">Retinitis pigmentosa 4, autosomal-dominant oder rezessiv<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.047,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_917\">\n                    <td style=\"\">RHO<\/td>\n                    <td style=\"\">Retinitis punctata albescens<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.047,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_918\">\n                    <td style=\"\">RHO<\/td>\n                    <td style=\"\">Nachtblindheit, kongenital station\u00e4r, autosomal dominant 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.047,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_919\">\n                    <td style=\"\">RLBP1<\/td>\n                    <td style=\"\">Bothnia Netzhautdysfunktion<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">954,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_920\">\n                    <td style=\"\">RLBP1<\/td>\n                    <td style=\"\">Retinis Punctata<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">954,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_921\">\n                    <td style=\"\">RLBP1<\/td>\n                    <td style=\"\">Zapfen-St\u00e4bchen-Dystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">954,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_922\">\n                    <td style=\"\">RLBP1<\/td>\n                    <td style=\"\">Fundus albipunctatus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">954,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_923\">\n                    <td style=\"\">RMRP<\/td>\n                    <td style=\"\">Dysplasie, anauxetische<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">0,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_924\">\n                    <td style=\"\">RMRP<\/td>\n                    <td style=\"\">Omenn-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">0,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_925\">\n                    <td style=\"\">RMRP<\/td>\n                    <td style=\"\">Kuorpel-Haar-Hypoplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">0,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_926\">\n                    <td style=\"\">RNASEH2B<\/td>\n                    <td style=\"\">Aicardi-Goutieres-Syndrom 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.068,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_927\">\n                    <td style=\"\">RNASET2<\/td>\n                    <td style=\"\">Zystische Leukoenzephalopathie ohne Megalenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">771,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_928\">\n                    <td style=\"\">ROBO3<\/td>\n                    <td style=\"\">Horizontale Blickparese mit Skoliose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.161,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_929\">\n                    <td style=\"\">ROGDI<\/td>\n                    <td style=\"\">Kohlsch\u00fctter-T\u00f6nz-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">864,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_930\">\n                    <td style=\"\">RP1<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.471,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_931\">\n                    <td style=\"\">RP1L1<\/td>\n                    <td style=\"\">Maculadystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">7.203,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_932\">\n                    <td style=\"\">RP2<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.053,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_933\">\n                    <td style=\"\">RPE65<\/td>\n                    <td style=\"\">autosomal rezessive Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.602,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_934\">\n                    <td style=\"\">RPE65<\/td>\n                    <td style=\"\">Leber Congenitale Amaurose 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.602,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_935\">\n                    <td style=\"\">RPE65<\/td>\n                    <td style=\"\">autosomal dominante Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.602,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_936\">\n                    <td style=\"\">RPGR<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.459,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_937\">\n                    <td style=\"\">RRM2B<\/td>\n                    <td style=\"\">Mitochondriales DNA Depletions Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.272,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_938\">\n                    <td style=\"\">RS1<\/td>\n                    <td style=\"\">Retinoschisis, X-chromosomale<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">675,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_939\">\n                    <td style=\"\">RSPH1<\/td>\n                    <td style=\"\">Kartagener-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">930,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_940\">\n                    <td style=\"\">RUNX2<\/td>\n                    <td style=\"\">Metaphyseale Dysplasie mit Kieferhypoplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.566,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_941\">\n                    <td style=\"\">RUNX2<\/td>\n                    <td style=\"\">Kleidokraniale Dysplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.566,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_942\">\n                    <td style=\"\">SAA1<\/td>\n                    <td style=\"\">Reaktives Amyloidose-Risiko (AS 52 und 57 im SAA1-Protein)<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">369,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_943\">\n                    <td style=\"\">SACS<\/td>\n                    <td style=\"\">autosomal rezessive spastische Ataxie Charlevoix-Saguenay<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">13.767,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_944\">\n                    <td style=\"\">SALL1<\/td>\n                    <td style=\"\">Townes-Brocks-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.975,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_945\">\n                    <td style=\"\">SALL1<\/td>\n                    <td style=\"\">Townes-Brocks branchiootorenal-like-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.975,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_946\">\n                    <td style=\"\">SALL4<\/td>\n                    <td style=\"\">IVIC-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.162,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_947\">\n                    <td style=\"\">SALL4<\/td>\n                    <td style=\"\">Duane-Radial Ray Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.162,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_948\">\n                    <td style=\"\">SAMHD1<\/td>\n                    <td style=\"\">Aicardi-Goutieres-Syndrom 5<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.881,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_949\">\n                    <td style=\"\">SAMHD1<\/td>\n                    <td style=\"\">Chilblain-Lupus 2<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.881,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_950\">\n                    <td style=\"\">SBDS<\/td>\n                    <td style=\"\">Shwachman-Diamond-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">753,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_951\">\n                    <td style=\"\">SCN1A<\/td>\n                    <td style=\"\">Famili\u00e4re hemiplegische Migr\u00e4ne Typ 3<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.030,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_952\">\n                    <td style=\"\">SCN1A<\/td>\n                    <td style=\"\">Generalisierte Epilepsie mit Fieberkr\u00e4mpfen Plus (GEFS+)<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.030,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_953\">\n                    <td style=\"\">SCN1B<\/td>\n                    <td style=\"\">Generalisierte Epilepsie mit Fieberkr\u00e4mpfen Plus (GEFS+)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">807,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_954\">\n                    <td style=\"\">SCN2A<\/td>\n                    <td style=\"\">Generalisierte Epilepsie mit Fieberkr\u00e4mpfen Plus (GEFS+)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.018,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_955\">\n                    <td style=\"\">SCN3A<\/td>\n                    <td style=\"\">Fokale Epilepsie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.003,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_956\">\n                    <td style=\"\">SCN4A<\/td>\n                    <td style=\"\">Paramyothonia congenita<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.511,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_957\">\n                    <td style=\"\">SCN4A<\/td>\n                    <td style=\"\">Myasthenes Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.511,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_958\">\n                    <td style=\"\">SCN8A<\/td>\n                    <td style=\"\">Fr\u00fchinfantile Epileptische Enzephalopathie (EIEE)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.943,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_959\">\n                    <td style=\"\">SCN9A<\/td>\n                    <td style=\"\">kongenitale Schmerzunempfindlichkeit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.967,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_960\">\n                    <td style=\"\">SCN9A<\/td>\n                    <td style=\"\">Erythromelalgie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.967,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_961\">\n                    <td style=\"\">SCN9A<\/td>\n                    <td style=\"\">Generalisierte Epilepsie mit Fieberkr\u00e4mpfen Plus (GEFS+)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.967,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_962\">\n                    <td style=\"\">SCN9A<\/td>\n                    <td style=\"\">Krankheit der Paroxysmalen extremen Schmerzen<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.967,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_963\">\n                    <td style=\"\">SCNN1B<\/td>\n                    <td style=\"\">Pseudohypoaldosteronismus, generalisierter, Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.923,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_964\">\n                    <td style=\"\">SCNN1G<\/td>\n                    <td style=\"\">Pseudohypoaldosteronismus, generalisierter, Typ 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.950,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_965\">\n                    <td style=\"\">SCP2<\/td>\n                    <td style=\"\">Leukoencephalopathy with dystonia and motor neuropathy<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.644,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_966\">\n                    <td style=\"\">SDHAF2<\/td>\n                    <td style=\"\">Paragangliomas 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">594,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_967\">\n                    <td style=\"\">SDHB<\/td>\n                    <td style=\"\">Carney-Stratakis-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">888,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_968\">\n                    <td style=\"\">SDHB<\/td>\n                    <td style=\"\">famili\u00e4res Phaeochromozytom-Paragangliom-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">888,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_969\">\n                    <td style=\"\">SDHB<\/td>\n                    <td style=\"\">Cowden-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">888,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_970\">\n                    <td style=\"\">SDHD<\/td>\n                    <td style=\"\">famili\u00e4res Phaeochromozytom-Paragangliom-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">480,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_971\">\n                    <td style=\"\">SDHD<\/td>\n                    <td style=\"\">Cowden-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">480,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_972\">\n                    <td style=\"\">SDHD<\/td>\n                    <td style=\"\">Carney-Stratakis-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">480,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_973\">\n                    <td style=\"\">SEMA3E<\/td>\n                    <td style=\"\">CHARGE Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.328,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_974\">\n                    <td style=\"\">SEPTIN9<\/td>\n                    <td style=\"\">Neuralgische Amyothrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.761,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_975\">\n                    <td style=\"\">SERPINC1<\/td>\n                    <td style=\"\">Thrombophilie mit Antithrombin III-Defizienz<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.395,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_976\">\n                    <td style=\"\">SERPING1<\/td>\n                    <td style=\"\">C1-Inhibitor-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.503,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_977\">\n                    <td style=\"\">SERPING1<\/td>\n                    <td style=\"\">Angi\u00f6dem, erblich, Typen I und II<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.503,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_978\">\n                    <td style=\"\">SETBP1<\/td>\n                    <td style=\"\">Schinzel-Giedion (midface retraction) -Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.791,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_979\">\n                    <td style=\"\">SETX<\/td>\n                    <td style=\"\">Amyotrophe Lateralsklerose (ALS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.034,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_980\">\n                    <td style=\"\">SETX<\/td>\n                    <td style=\"\">Spinocerebell\u00e4re Ataxie mit axonaler Neuropathie Typ 2\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.034,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_981\">\n                    <td style=\"\">SFTPB<\/td>\n                    <td style=\"\">Akute neonatale Atemnot durch SP-B-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.146,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_982\">\n                    <td style=\"\">SFTPB<\/td>\n                    <td style=\"\">Kongenitale Alveolarproteinose (Surfactant-Protein B-Defizienz; SFTPBGen)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.146,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_983\">\n                    <td style=\"\">SFTPC<\/td>\n                    <td style=\"\">Interstitielle Lungenerkrankung durch SP-C-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">594,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_984\">\n                    <td style=\"\">SGCE<\/td>\n                    <td style=\"\">Myklonus Dystonie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.503,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_985\">\n                    <td style=\"\">SGSH<\/td>\n                    <td style=\"\">Mukopolysaccharidose Typ 3A \/ Sanfilippo-Krankheit Typ A<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.509,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_986\">\n                    <td style=\"\">SH2D1A<\/td>\n                    <td style=\"\">Lymphoproliferative Erkrankung, X-chromosomal<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">387,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_987\">\n                    <td style=\"\">SHH<\/td>\n                    <td style=\"\">Schizenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.389,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_988\">\n                    <td style=\"\">SHH<\/td>\n                    <td style=\"\">Mikrophthalmie mit Kolobom 5<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.389,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_989\">\n                    <td style=\"\">SHH<\/td>\n                    <td style=\"\">Syndrom des einzelnen maxill\u00e4ren mittleren Schneidezahns<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.389,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_990\">\n                    <td style=\"\">SHH<\/td>\n                    <td style=\"\">Holoprosenzephalie 3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.389,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_991\">\n                    <td style=\"\">SHH<\/td>\n                    <td style=\"\">Schizenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.389,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_992\">\n                    <td style=\"\">SIL1<\/td>\n                    <td style=\"\">Marinesco-Sj\u00f6gren-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.386,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_993\">\n                    <td style=\"\">SIX3<\/td>\n                    <td style=\"\">Holoprosenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">999,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_994\">\n                    <td style=\"\">SIX3<\/td>\n                    <td style=\"\">Schizenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">999,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_995\">\n                    <td style=\"\">SIX3<\/td>\n                    <td style=\"\">Schizenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">999,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_996\">\n                    <td style=\"\">SLC12A3<\/td>\n                    <td style=\"\">Gitelman-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.093,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_997\">\n                    <td style=\"\">SLC12A5<\/td>\n                    <td style=\"\">Epileptische Enzephalopathie, fr\u00fchkindlich, 34<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.420,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_998\">\n                    <td style=\"\">SLC16A12<\/td>\n                    <td style=\"\">heredit\u00e4re Katarakt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.551,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_999\">\n                    <td style=\"\">SLC17A5<\/td>\n                    <td style=\"\">Sialins\u00e4ure-Speicherkrankheit (Salla-Krankheit)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.488,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1000\">\n                    <td style=\"\">SLC19A3<\/td>\n                    <td style=\"\">Biotin-responsive St\u00f6rung der Basalganglien<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.527,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1001\">\n                    <td style=\"\">SLC1A3<\/td>\n                    <td style=\"\">Episodische Ataxie Typ 6<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.770,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1002\">\n                    <td style=\"\">SLC22A5<\/td>\n                    <td style=\"\">Carnitin-Defizienz, systemisch prim\u00e4r<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.746,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1003\">\n                    <td style=\"\">SLC25A15<\/td>\n                    <td style=\"\">HHH-Syndrom (Hyperornithin\u00e4mie, Hyperammon\u00e4mie, Homocitrullinurie)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">906,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1004\">\n                    <td style=\"\">SLC25A19<\/td>\n                    <td style=\"\">progressive demyelinisierende  Polyneuropathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">963,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1005\">\n                    <td style=\"\">SLC25A22<\/td>\n                    <td style=\"\">fr\u00fchinfantile epileptische Enzephalopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">972,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1006\">\n                    <td style=\"\">SLC25A3<\/td>\n                    <td style=\"\">Kardiomyopathie - Hypotonie - Laktazidose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.089,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1007\">\n                    <td style=\"\">SLC26A2<\/td>\n                    <td style=\"\">Multiple epiphys\u00e4re Dysplasie\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.220,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1008\">\n                    <td style=\"\">SLC26A4<\/td>\n                    <td style=\"\">Pendred-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.343,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1009\">\n                    <td style=\"\">SLC26A5<\/td>\n                    <td style=\"\">autosomal-rezessive nicht-syndromale sensorineurale Schwerh\u00f6rigkeit, Typ DFNB<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.241,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1010\">\n                    <td style=\"\">SLC2A1<\/td>\n                    <td style=\"\">GLUT1 Defizienz-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.479,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1011\">\n                    <td style=\"\">SLC2A10<\/td>\n                    <td style=\"\">Syndrom der geschl\u00e4ngelten Arterien (ATS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.626,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1012\">\n                    <td style=\"\">SLC30A10<\/td>\n                    <td style=\"\">Zirrhose-Dystonie-Polyzyth\u00e4mie-Hypermagnesi\u00e4mie-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.458,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1013\">\n                    <td style=\"\">SLC35A1<\/td>\n                    <td style=\"\">Kongenitale Glykosylierungserkrankungen, Typ IIf<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.014,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1014\">\n                    <td style=\"\">SLC35D1<\/td>\n                    <td style=\"\">Schneckenbecken-Dysplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.068,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1015\">\n                    <td style=\"\">SLC36A2<\/td>\n                    <td style=\"\">Iminoglyzinurie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.452,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1016\">\n                    <td style=\"\">SLC3A1<\/td>\n                    <td style=\"\">Cystinuria<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.058,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1017\">\n                    <td style=\"\">SLC40A1<\/td>\n                    <td style=\"\">H\u00e4mochromatose Typ 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.716,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1018\">\n                    <td style=\"\">SLC45A2<\/td>\n                    <td style=\"\">Okulokutaner Albinismus Typ IV<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.593,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1019\">\n                    <td style=\"\">SLC46A1<\/td>\n                    <td style=\"\">Hereditary Folate Malabsorption<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.380,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1020\">\n                    <td style=\"\">SLC4A1<\/td>\n                    <td style=\"\">Sph\u00e4rozytose, Typ 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.736,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1021\">\n                    <td style=\"\">SLC4A1<\/td>\n                    <td style=\"\">Ovalozytoe, s\u00fcdostasiatische<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.736,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1022\">\n                    <td style=\"\">SLC4A1<\/td>\n                    <td style=\"\">Azidose, renale tubul\u00e4re, mit An\u00e4mie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.736,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1023\">\n                    <td style=\"\">SLC4A1<\/td>\n                    <td style=\"\">Azidose, renale tubul\u00e4re, autosomal-dominante Form<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.736,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1024\">\n                    <td style=\"\">SLC5A5<\/td>\n                    <td style=\"\">Schilddr\u00fcsen Dyshormonogenese, famili\u00e4re<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.932,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1025\">\n                    <td style=\"\">SLC5A6<\/td>\n                    <td style=\"\">Assoziierung mit Gehirn-, Immun-, Knochen- und Darm-St\u00f6rungen bei Kleinkindern<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.908,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1026\">\n                    <td style=\"\">SLC6A1<\/td>\n                    <td style=\"\">MYOCLONIC-ATONIC EPILEPSY; MAE<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.872,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1027\">\n                    <td style=\"\">SLC6A20<\/td>\n                    <td style=\"\">Iminoglyzinurie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.812,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1028\">\n                    <td style=\"\">SLC6A20<\/td>\n                    <td style=\"\">Hyperglyzinurie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.812,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1029\">\n                    <td style=\"\">SLC6A3<\/td>\n                    <td style=\"\">Infantiles Dystonie-Parkinson-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.863,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1030\">\n                    <td style=\"\">SLC6A5<\/td>\n                    <td style=\"\">heredit\u00e4re Hyperekplexie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.394,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1031\">\n                    <td style=\"\">SLC6A8<\/td>\n                    <td style=\"\">Kreatin-Transporter-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.908,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1032\">\n                    <td style=\"\">SMAD4<\/td>\n                    <td style=\"\">Generalisierte juvenile Polyposis \/ juvenile polyposis coli<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.740,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1033\">\n                    <td style=\"\">SMAD4<\/td>\n                    <td style=\"\">Juveniles Polyposis-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.740,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1034\">\n                    <td style=\"\">SMAD4<\/td>\n                    <td style=\"\">Myhre-syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.740,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1035\">\n                    <td style=\"\">SMC1A<\/td>\n                    <td style=\"\">Cornelia de Lange Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.702,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1036\">\n                    <td style=\"\">SMC3<\/td>\n                    <td style=\"\">Cornelia de Lange Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.654,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1037\">\n                    <td style=\"\">SMPD1<\/td>\n                    <td style=\"\">Niemann Pick Erkrankung Typ A \/ Typ B<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.896,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1038\">\n                    <td style=\"\">SMS<\/td>\n                    <td style=\"\">X-chromosomale geistige Retardierung,Typ Snyder<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.101,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1039\">\n                    <td style=\"\">SNAP29<\/td>\n                    <td style=\"\">CEDNIK-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">777,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1040\">\n                    <td style=\"\">SNCA<\/td>\n                    <td style=\"\">Parkinson Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">480,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1041\">\n                    <td style=\"\">SNORD118<\/td>\n                    <td style=\"\">Leukenzephalopathie mit Kalzifikation und Cysten<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">0,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1042\">\n                    <td style=\"\">SOX10<\/td>\n                    <td style=\"\">Waardenburg-Syndrom Typ 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.617,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1043\">\n                    <td style=\"\">SOX10<\/td>\n                    <td style=\"\">Waardenburg-Syndrom Typ 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.617,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1044\">\n                    <td style=\"\">SOX3<\/td>\n                    <td style=\"\">Panhypopituarismus, X-gekoppelt<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.341,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1045\">\n                    <td style=\"\">SOX3<\/td>\n                    <td style=\"\">Geistige Retardierung, X-chromosomale mit isoliertem Wachstumshormonmangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.341,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1046\">\n                    <td style=\"\">SPAST<\/td>\n                    <td style=\"\">Spastische Paraplegie Typ 4<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.956,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1047\">\n                    <td style=\"\">SPATA5<\/td>\n                    <td style=\"\">Epilepsy, hearing loss and mental retardation Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.751,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1048\">\n                    <td style=\"\">SPG11<\/td>\n                    <td style=\"\">Spastische Paraplegie Typ 11<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">7.332,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1049\">\n                    <td style=\"\">SPG7<\/td>\n                    <td style=\"\">Spastische Paraplegie Typ 7<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.430,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1050\">\n                    <td style=\"\">SPINK1<\/td>\n                    <td style=\"\">Tropische Pankreatitis<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">240,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1051\">\n                    <td style=\"\">SPINK1<\/td>\n                    <td style=\"\">Pankreatitis, erblich<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">240,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1052\">\n                    <td style=\"\">SPR<\/td>\n                    <td style=\"\">Dopa-Responsive Dyst. due to Sepiapterin Red. Deficiency<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">786,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1053\">\n                    <td style=\"\">SPRED1<\/td>\n                    <td style=\"\">Neurofibromatose 1-\u00e4hnliches Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.335,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1054\">\n                    <td style=\"\">SPTAN1<\/td>\n                    <td style=\"\">fr\u00fchinfantile epileptische Enzephalopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">7.521,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1055\">\n                    <td style=\"\">SPTLC1<\/td>\n                    <td style=\"\">autonome heredit\u00e4re sensorische Neuropathie Typ1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.542,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1056\">\n                    <td style=\"\">SRCAP<\/td>\n                    <td style=\"\">Floating-Harbor-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">9.693,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1057\">\n                    <td style=\"\">SRPX2<\/td>\n                    <td style=\"\">Rolando Epilepsie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.398,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1058\">\n                    <td style=\"\">ST3GAL3<\/td>\n                    <td style=\"\">Epileptische Enzephalopathie, fr\u00fchkindlich, 15<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.362,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1059\">\n                    <td style=\"\">ST3GAL3<\/td>\n                    <td style=\"\">Geistige Retardierung, autosomal rezessiv 12<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.362,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1060\">\n                    <td style=\"\">STAT3<\/td>\n                    <td style=\"\">AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.409,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1061\">\n                    <td style=\"\">STAT3<\/td>\n                    <td style=\"\">HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.409,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1062\">\n                    <td style=\"\">STING1<\/td>\n                    <td style=\"\">STING-assoziierte Vaskulopathie mit Beginn in der Kindheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.140,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1063\">\n                    <td style=\"\">STING1<\/td>\n                    <td style=\"\">Chilblain-Lupus, famili\u00e4rer<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.140,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1064\">\n                    <td style=\"\">STK11<\/td>\n                    <td style=\"\">Peutz-Jeghers-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.803,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1065\">\n                    <td style=\"\">STUB1<\/td>\n                    <td style=\"\">Ataxie, spinozerebell\u00e4re, Typ 16, autosomal rezessiv<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">912,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1066\">\n                    <td style=\"\">STX16<\/td>\n                    <td style=\"\">Pseudohypoparathyreodismus Ib<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">978,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1067\">\n                    <td style=\"\">STXBP1<\/td>\n                    <td style=\"\">fr\u00fchinfantile epileptische  Enzephalopathie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.812,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1068\">\n                    <td style=\"\">SUFU<\/td>\n                    <td style=\"\">Medullablastom, desmoplastisch<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.455,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1069\">\n                    <td style=\"\">SUFU<\/td>\n                    <td style=\"\">Basalzelln\u00e4vus \/ Gorlin-Sydrom \/ Gorlin-Goltz-Syndrom \/ N\u00e4voides Basalzellkarzinom-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.455,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1070\">\n                    <td style=\"\">SUOX<\/td>\n                    <td style=\"\">Sulfitoxidase-Mangel<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.638,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1071\">\n                    <td style=\"\">SYN1<\/td>\n                    <td style=\"\">Epilepsie, X-gekoppelt, mit Lernbehinderung und Verhaltensauff\u00e4lligkeiten<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.118,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1072\">\n                    <td style=\"\">SYNGAP1<\/td>\n                    <td style=\"\">Intelligenzminderung, nicht-syndromale, autosomal-dominante<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.032,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1073\">\n                    <td style=\"\">TARDBP<\/td>\n                    <td style=\"\">Amyotrophe Lateralsklerose (ALS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.245,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1074\">\n                    <td style=\"\">TBK1<\/td>\n                    <td style=\"\">Frontotemporale Demenz und \/ oder Amyotrophe Lateralsklerose 4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.190,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1075\">\n                    <td style=\"\">TBP<\/td>\n                    <td style=\"\">Ataxie, spinozerebell\u00e4re, Typ 17<\/td>\n                    <td style=\"\">Repeat-Expansions-Analyse<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.020,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1076\">\n                    <td style=\"\">TCF4<\/td>\n                    <td style=\"\">Pitt-Hopkins Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.322,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1077\">\n                    <td style=\"\">TCOF1<\/td>\n                    <td style=\"\">Treacher Collins Syndrom\u00a0<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.470,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1078\">\n                    <td style=\"\">TECTA<\/td>\n                    <td style=\"\">nicht-syndromale sensorineurale autosomal-dominante Schwerh\u00f6rigkeit, Typ DFNA<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.468,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1079\">\n                    <td style=\"\">TECTA<\/td>\n                    <td style=\"\">nicht-syndromale sensorineurale autosomal-rezessive Schwerh\u00f6rigkeit, Typ DFNB<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.468,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1080\">\n                    <td style=\"\">TEK<\/td>\n                    <td style=\"\">Fehlbildung, mukokutane ven\u00f6se<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.375,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1081\">\n                    <td style=\"\">TG<\/td>\n                    <td style=\"\">Schilddr\u00fcsen Dyshormonogenese 3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">8.307,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1082\">\n                    <td style=\"\">TGIF1<\/td>\n                    <td style=\"\">Holoprosenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">861,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1083\">\n                    <td style=\"\">TH<\/td>\n                    <td style=\"\">Dopa-responsive Dystonie THD<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.587,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1084\">\n                    <td style=\"\">THAP1<\/td>\n                    <td style=\"\">Dystonie, DYT6, prim\u00e4re<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">642,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1085\">\n                    <td style=\"\">THRB<\/td>\n                    <td style=\"\">THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE; GRTH<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.386,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1086\">\n                    <td style=\"\">THRB<\/td>\n                    <td style=\"\">THYROID HORMONE RESISTANCE, SELECTIVE PITUITARY; PRTH<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.386,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1087\">\n                    <td style=\"\">THRB<\/td>\n                    <td style=\"\">THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT; GRTH<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.386,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1088\">\n                    <td style=\"\">TIA1<\/td>\n                    <td style=\"\">distale Myopathie, Typ Welander<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.161,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1089\">\n                    <td style=\"\">TIMM8A<\/td>\n                    <td style=\"\">Taubheit\u00a0Optikusatrophie Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">294,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1090\">\n                    <td style=\"\">TIMM8A<\/td>\n                    <td style=\"\">Deafness-Dystonia-Syndrom Mohr-Tranebjaerg-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">294,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1091\">\n                    <td style=\"\">TK2<\/td>\n                    <td style=\"\">Mitochondriales DNA-Depletionssyndrom, myopathische Form<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">798,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1092\">\n                    <td style=\"\">TMEM106B<\/td>\n                    <td style=\"\">Frontotemporale Demenz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">825,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1093\">\n                    <td style=\"\">TMEM126A<\/td>\n                    <td style=\"\">Optikusatrophie Typ 7<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">588,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1094\">\n                    <td style=\"\">TMEM165<\/td>\n                    <td style=\"\">CDG-Syndrom 2K<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">975,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1095\">\n                    <td style=\"\">TMEM43<\/td>\n                    <td style=\"\">Famili\u00e4re isolierte arrhythmogene ventrikul\u00e4re Kardiomyopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.203,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1096\">\n                    <td style=\"\">TNC<\/td>\n                    <td style=\"\">Schwerh\u00f6rigkeit, autosomal-dominant, Typ 56<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">6.606,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1097\">\n                    <td style=\"\">TNFAIP3<\/td>\n                    <td style=\"\">Behcet-\u00e4hnliche Krankheit des Kindes, heredit\u00e4re<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.373,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1098\">\n                    <td style=\"\">TNFRSF1A<\/td>\n                    <td style=\"\">Periodisches Fieber, famili\u00e4r<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.368,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1099\">\n                    <td style=\"\">TNFRSF1A<\/td>\n                    <td style=\"\">TNF-Rezeptor 1-assoziiertes periodisches Syndrom (TRAPS; Exons 2, 3, 4, 6 und 7 des TNFRSF1A-Gens)<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.368,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1100\">\n                    <td style=\"\">TNNT2<\/td>\n                    <td style=\"\">Kardiomyopathie, dilatative  (DCM)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.107,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1101\">\n                    <td style=\"\">TNNT2<\/td>\n                    <td style=\"\">Hypertrophe Kardiomyopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.107,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1102\">\n                    <td style=\"\">TNNT2<\/td>\n                    <td style=\"\">restriktive famili\u00e4re isolierte  Kardiomyopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.107,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1103\">\n                    <td style=\"\">TOMM40<\/td>\n                    <td style=\"\">Alzheimer Disease, late-onset<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.086,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1104\">\n                    <td style=\"\">TOR1A<\/td>\n                    <td style=\"\">Dystonie, DYT1, prim\u00e4re<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">999,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1105\">\n                    <td style=\"\">TPM2<\/td>\n                    <td style=\"\">Nemalin-Myopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">855,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1106\">\n                    <td style=\"\">TPP1<\/td>\n                    <td style=\"\">Neuronale Ceroid-Lipofuszinose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.692,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1107\">\n                    <td style=\"\">TRAPPC10<\/td>\n                    <td style=\"\">Holoprosenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.780,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1108\">\n                    <td style=\"\">TRAPPC2<\/td>\n                    <td style=\"\">Spondyloepiphys\u00e4re Dysplasie\u00a0<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">525,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1109\">\n                    <td style=\"\">TREM2<\/td>\n                    <td style=\"\">polyzystische lipomembran\u00f6se Osteodysplasie mit sklerosierender Leukenzephalopathie (PLOSL)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">693,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1110\">\n                    <td style=\"\">TREX1<\/td>\n                    <td style=\"\">Aicardi-Goutieres-Syndrom 1, dominant und rezessiv<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">945,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1111\">\n                    <td style=\"\">TREX1<\/td>\n                    <td style=\"\">Retinale Vaskulopathie mit cerebraler Leukodystrophie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">945,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1112\">\n                    <td style=\"\">TREX1<\/td>\n                    <td style=\"\">Chilblain-Lupus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">945,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1113\">\n                    <td style=\"\">TRPM1<\/td>\n                    <td style=\"\">Kongenitale station\u00e4re Nachtblindheit<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.929,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1114\">\n                    <td style=\"\">TRPS1<\/td>\n                    <td style=\"\">Langer-Giedion Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.885,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1115\">\n                    <td style=\"\">TRPS1<\/td>\n                    <td style=\"\">Tricho-rhino-phalangealen Syndrome (TRPS) Typ 3<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.885,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1116\">\n                    <td style=\"\">TRPS1<\/td>\n                    <td style=\"\">Tricho-rhino-phalangealen Syndrome (TRPS) Typ 1<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.885,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1117\">\n                    <td style=\"\">TRPV4<\/td>\n                    <td style=\"\">Heredit\u00e4re motorische und sensorische Neuropathie 2C<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.616,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1118\">\n                    <td style=\"\">TRPV4<\/td>\n                    <td style=\"\">Charcot-Marie-Tooth--Krankheit Typ 2C<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.616,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1119\">\n                    <td style=\"\">TSC1<\/td>\n                    <td style=\"\">Tuber\u00f6se Sklerose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.495,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1120\">\n                    <td style=\"\">TSC2<\/td>\n                    <td style=\"\">Tuber\u00f6se Sklerose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.514,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1121\">\n                    <td style=\"\">TSEN54<\/td>\n                    <td style=\"\">Pontocerebell\u00e4re Hypoplasie Typ 2A<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.794,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1122\">\n                    <td style=\"\">TSHB<\/td>\n                    <td style=\"\">HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4; CHNG4<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">417,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1123\">\n                    <td style=\"\">TSHR<\/td>\n                    <td style=\"\">Hypothyroidismus, kongenital, nongoitr\u00f6s 1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.295,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1124\">\n                    <td style=\"\">TSHR<\/td>\n                    <td style=\"\">Hypothyroidismus, famil\u00e4re Schwangerschaft<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.295,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1125\">\n                    <td style=\"\">TSHR<\/td>\n                    <td style=\"\">Hypothyroidismus, nicht-autoimmun<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.295,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1126\">\n                    <td style=\"\">TSPAN12<\/td>\n                    <td style=\"\">Famili\u00e4re exsudativen Retinopathie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">918,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1127\">\n                    <td style=\"\">TTC8<\/td>\n                    <td style=\"\">Bardet Biedl Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.596,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1128\">\n                    <td style=\"\">TTC8<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.596,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1129\">\n                    <td style=\"\">TTR<\/td>\n                    <td style=\"\">Heredit\u00e4re Transthyretinamyloidose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">444,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1130\">\n                    <td style=\"\">TUBA1A<\/td>\n                    <td style=\"\">Lissenzephalie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.356,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1131\">\n                    <td style=\"\">TUBA8<\/td>\n                    <td style=\"\">Polymikrogyrie mit Sehnerv-Hypoplasie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.350,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1132\">\n                    <td style=\"\">TUBB2B<\/td>\n                    <td style=\"\">Polymicrogyrie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.338,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1133\">\n                    <td style=\"\">TUBB3<\/td>\n                    <td style=\"\">Kongenitale extraokul\u00e4re Muskelfibrose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.353,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1134\">\n                    <td style=\"\">TUBB4A<\/td>\n                    <td style=\"\">Dystonie 4, Torsion, autosomal-dominant<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.488,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1135\">\n                    <td style=\"\">TUBB4A<\/td>\n                    <td style=\"\">Leukodystrophie, hypomyelisierend, Typ 6<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.488,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1136\">\n                    <td style=\"\">TULP1<\/td>\n                    <td style=\"\">Retinitis pigmentosa<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.629,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1137\">\n                    <td style=\"\">TULP1<\/td>\n                    <td style=\"\">Leber Congenitale Amaurose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.629,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1138\">\n                    <td style=\"\">TWIST1<\/td>\n                    <td style=\"\">Saethre-Chotzen-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">609,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1139\">\n                    <td style=\"\">TWNK<\/td>\n                    <td style=\"\">Externe progressive Ophthalmoplegie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.055,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1140\">\n                    <td style=\"\">TWNK<\/td>\n                    <td style=\"\">Externe progressive Ophthalmoplegie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.055,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1141\">\n                    <td style=\"\">TYR<\/td>\n                    <td style=\"\">Okulokutaner Albinismus Typ I<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.590,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1142\">\n                    <td style=\"\">TYROBP<\/td>\n                    <td style=\"\">polyzystische lipomembran\u00f6se Osteodysplasie mit sklerosierender Leukenzephalopathie (PLOSL)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">342,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1143\">\n                    <td style=\"\">TYRP1<\/td>\n                    <td style=\"\">Okulokutaner Albinismus Typ III<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.614,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1144\">\n                    <td style=\"\">UBE3A<\/td>\n                    <td style=\"\">Angelman Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.628,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1145\">\n                    <td style=\"\">UBQLN2<\/td>\n                    <td style=\"\">ALS mit oder ohne frontotemporale Demenz<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.875,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1146\">\n                    <td style=\"\">UGT1A1<\/td>\n                    <td style=\"\">Morbus Gilbert-Meulengracht<\/td>\n                    <td style=\"\">Sequenzierung Hotspots<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.602,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1147\">\n                    <td style=\"\">UNC13D<\/td>\n                    <td style=\"\">Lymphohistiozytose, h\u00e4mophagozytische, famili\u00e4re Form 3<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.273,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1148\">\n                    <td style=\"\">UPK3A<\/td>\n                    <td style=\"\">bilaterale Nierenagenesie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">864,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1149\">\n                    <td style=\"\">UPK3A<\/td>\n                    <td style=\"\">Kongenitale Anomalien der Niere und des Urogenitaltrakts, Pr\u00e4disposition f\u00fcr, CAKUT<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">864,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1150\">\n                    <td style=\"\">UPK3A<\/td>\n                    <td style=\"\">M\u00f6glicherweise verkn\u00fcpft mit Anomalien der Niere und des Urogenitaltrakts<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">864,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1151\">\n                    <td style=\"\">USH2A<\/td>\n                    <td style=\"\">Usher Syndrom Typ 2A<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">15.681,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1152\">\n                    <td style=\"\">USP8<\/td>\n                    <td style=\"\">M\u00f6glicherweise verkn\u00fcpft mit spastischer Paraplegie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.357,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1153\">\n                    <td style=\"\">USP8<\/td>\n                    <td style=\"\">Spastische Paraplegie, Typ 59<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.357,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1154\">\n                    <td style=\"\">VAPB<\/td>\n                    <td style=\"\">Amyotrophe Lateralsklerose (ALS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">732,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1155\">\n                    <td style=\"\">VCAN<\/td>\n                    <td style=\"\">Wagner Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">10.191,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1156\">\n                    <td style=\"\">VCP<\/td>\n                    <td style=\"\">Amyotrophe Lateralsklerose (ALS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.421,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1157\">\n                    <td style=\"\">VHL<\/td>\n                    <td style=\"\">Chuvash-Erythrozytose<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">753,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1158\">\n                    <td style=\"\">VHL<\/td>\n                    <td style=\"\">von-Hippel-Lindau (VHL)-Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">753,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1159\">\n                    <td style=\"\">VLDLR<\/td>\n                    <td style=\"\">Dys\u00e4quilibrium-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.622,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1160\">\n                    <td style=\"\">VPS13A<\/td>\n                    <td style=\"\">Choreoakanthozytose<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">9.525,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1161\">\n                    <td style=\"\">VPS13B<\/td>\n                    <td style=\"\">Cohen Syndrom<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">12.069,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1162\">\n                    <td style=\"\">VPS35<\/td>\n                    <td style=\"\">Parkinsonkrankheit 17<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.391,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1163\">\n                    <td style=\"\">VRK1<\/td>\n                    <td style=\"\">Pontocerebell\u00e4re Hypoplasie Typ1<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.347,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1164\">\n                    <td style=\"\">WDR35<\/td>\n                    <td style=\"\">Kurzrippen-Dysplasie 7 mit oder ohne Polydaktylie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.546,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1165\">\n                    <td style=\"\">WDR35<\/td>\n                    <td style=\"\">Kranioektodermale Dysplasie 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.546,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1166\">\n                    <td style=\"\">WDR45<\/td>\n                    <td style=\"\">Neurodegeneration mit Eisenablagerung im Gehirn (NBIA)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.086,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1167\">\n                    <td style=\"\">WDR62<\/td>\n                    <td style=\"\">Mikrozephalie, prim\u00e4r, autosomal-rezessiv, mit oder ohne kortikale Verformung<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">4.572,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1168\">\n                    <td style=\"\">WDR73<\/td>\n                    <td style=\"\">Galloway-Mowat-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.137,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1169\">\n                    <td style=\"\">WDR81<\/td>\n                    <td style=\"\">Zerebell\u00e4re Ataxie, Mentale Retardierung und Dis\u00e4quilibrium Syndrom 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">5.826,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1170\">\n                    <td style=\"\">WFS1<\/td>\n                    <td style=\"\">Wolfram Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.709,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1171\">\n                    <td style=\"\">WHRN<\/td>\n                    <td style=\"\">autosomal-rezessive nicht-syndromale sensorineurale Schwerh\u00f6rigkeit, Typ DFNB<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.724,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1172\">\n                    <td style=\"\">WIPF1<\/td>\n                    <td style=\"\">Wiskott-Aldrich-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.533,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1173\">\n                    <td style=\"\">WNT4<\/td>\n                    <td style=\"\">SERKAL-Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.056,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1174\">\n                    <td style=\"\">WNT4<\/td>\n                    <td style=\"\">M\u00fcller-Gang Aplasie und Hyperandrogenismus<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.056,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1175\">\n                    <td style=\"\">XIAP<\/td>\n                    <td style=\"\">Lymphoproliferatives Syndrom, X-gekoppelt, 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.494,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1176\">\n                    <td style=\"\">XK<\/td>\n                    <td style=\"\">McLeod Neuro-Akanthozytose-Syndrom (MLS)<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.335,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1177\">\n                    <td style=\"\">XPR1<\/td>\n                    <td style=\"\">Basalganglien-Kalzifizierung, idiopathisch, 6<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.091,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1178\">\n                    <td style=\"\">XYLT1<\/td>\n                    <td style=\"\">Desbuquois-Dysplasie 2<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">2.880,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1179\">\n                    <td style=\"\">ZC4H2<\/td>\n                    <td style=\"\">Wieacker-Wolf Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">675,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1180\">\n                    <td style=\"\">ZEB2<\/td>\n                    <td style=\"\">Mowat Wilson Syndrom<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.645,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1181\">\n                    <td style=\"\">ZFPM2<\/td>\n                    <td style=\"\">Fallot-Tetralogie<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">3.456,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1182\">\n                    <td style=\"\">ZFYVE26<\/td>\n                    <td style=\"\">Spastische Paraplegie Typ 15<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">7.665,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1183\">\n                    <td style=\"\">ZIC1<\/td>\n                    <td style=\"\">Kraniosynostosen 6<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR)<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.344,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1184\">\n                    <td style=\"\">ZIC2<\/td>\n                    <td style=\"\">Holoprosenzephalie<\/td>\n                    <td style=\"\">Deletions-\/Duplikationsanalyse (MLPA \/ qPCR);Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.599,00<\/td>\n            <\/tr>\n            <tr id=\"table_42_row_1185\">\n                    <td style=\"\">ZIC4<\/td>\n                    <td style=\"\">Dany Walker Malformation<\/td>\n                    <td style=\"\">Sequenzierung aller kodierender Exons des Gens<\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\"><\/td>\n                    <td style=\"\">1.155,00<\/td>\n            <\/tr>\n    <\/tbody>        <!-- \/Table body -->\n\n        \n    <\/table>\n\n        <span class=\"powered_by_link d-block m-l-10 m-t-10 m-b-10\">Generated by <a href=\"https:\/\/wpdatatables.com\" rel=\"nofollow\" target=\"_blank\">wpDataTables<\/a><\/span>\n<\/div><style>\ntable.wpDataTable { table-layout: fixed !important; }\ntable.wpDataTable td, table.wpDataTable th { white-space: normal !important; }\ntable.wpDataTable td.numdata { text-align: right !important; }\n.wpDataTablesWrapper table.wpDataTable > tbody > tr > td{ border: none !important; }\n.wpDataTablesWrapper table.wpDataTable > thead > tr > th{ border: none !important; }\n<\/style>\n<style>\n        \/* table font color *\/\n    .wpdt-c.wpDataTablesWrapper table.wpdtSimpleTable thead th,\n    .wpdt-c.wpDataTablesWrapper 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3px;--awb-inner-bg-overflow:hidden;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:0px;--awb-spacing-left-small:0px;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><span class=\"fusion-column-inner-bg hover-type-none\"><a class=\"fusion-column-anchor\" href=\"#awb-open-oc__62989\"><span class=\"fusion-column-inner-bg-image\"><\/span><\/a><\/span><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"df-element dvcss dvcss_e_eyJzb3VyY2UiOiJcL3dwLWNvbnRlbnRcL3VwbG9hZHNcLzIwMjNcLzAzXC9DZUdhVF9FaW5zZW5kZWZvcm11bGFyX0ROQV9EaWFnbm9zdGlrLnBkZiIsInBkZlRodW1iIjoiXC93cC1jb250ZW50XC91cGxvYWRzXC9kZWFycGRmLXRodW1ic1wvMTYwMTMuanBlZyIsImF1dG9PcGVuT3V0bGluZSI6ZmFsc2UsImF1dG9PcGVuVGh1bWJuYWlsIjpmYWxzZSwic2x1ZyI6IjE2MDEzIiwiaWQiOjE2MDEzLCJsaWdodGJveCI6InRodW1iIn0=  \">Einsendeformular Molecular Diagnostics<\/div><script class=\"df-shortcode-script\" type=\"application\/javascript\">if(window.DEARPDF && window.DEARPDF.parseElements){window.DEARPDF.parseElements();}<\/script><\/div><\/div><\/div><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column 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style=\"--awb-bg-size:cover;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:50%;--awb-order-small:0;--awb-spacing-right-small:3.84%;--awb-spacing-left-small:3.84%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-19 fusion_builder_column_inner_1_1 1_1 fusion-flex-column fusion-flex-align-self-stretch fusion-column-inner-bg-wrapper fusion-animated\" style=\"--awb-overflow:hidden;--awb-inner-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-inner-bg-border-radius:3px 3px 3px 3px;--awb-inner-bg-overflow:hidden;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:0px;--awb-spacing-left-small:0px;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><span class=\"fusion-column-inner-bg hover-type-none\"><a class=\"fusion-column-anchor\" href=\"#awb-open-oc__63006\"><span class=\"fusion-column-inner-bg-image\"><\/span><\/a><\/span><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"df-element dvcss dvcss_e_eyJzb3VyY2UiOiJcL3dwLWNvbnRlbnRcL3VwbG9hZHNcLzIwMjNcLzA0XC9DZUdhVF9FaW5zZW5kZWZvcm11bGFyX1NlZ3JlZ2F0aW9uc2FuYWx5c2UucGRmIiwicGRmVGh1bWIiOiJcL3dwLWNvbnRlbnRcL3VwbG9hZHNcL2RlYXJwZGYtdGh1bWJzXC8yMDA2OC5qcGVnIiwiYXV0b09wZW5PdXRsaW5lIjpmYWxzZSwiYXV0b09wZW5UaHVtYm5haWwiOmZhbHNlLCJzbHVnIjoiMjAwNjgiLCJpZCI6MjAwNjgsImxpZ2h0Ym94IjoidGh1bWIifQ==  \">Einsendeformular Segregationsanalyse<\/div><script class=\"df-shortcode-script\" type=\"application\/javascript\">if(window.DEARPDF && window.DEARPDF.parseElements){window.DEARPDF.parseElements();}<\/script><\/div><\/div><\/div><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-20 fusion_builder_column_inner_1_1 1_1 fusion-flex-column\" style=\"--awb-padding-left:10px;--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><a class=\"fusion-modal-text-link\" id=\"EF_SEG\" href=\"#\">Einsendeformular Segregationsanalyse herunterladen<\/a><\/div><\/div><\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-18 fusion_builder_column_1_4 1_4 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:50%;--awb-order-small:0;--awb-spacing-right-small:3.84%;--awb-spacing-left-small:3.84%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-21 fusion_builder_column_inner_1_1 1_1 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-overflow:hidden;--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:0px;--awb-spacing-left-small:0px;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"df-element dvcss dvcss_e_eyJzb3VyY2UiOiJcL3dwLWNvbnRlbnRcL3VwbG9hZHNcLzIwMjNcLzAzXC9DZUdhVF9Gb3JtdWxhcl9QcmFlZGlrdGl2ZV9EaWFnbm9zdGlrLnBkZiIsInBkZlRodW1iIjoiXC93cC1jb250ZW50XC91cGxvYWRzXC9kZWFycGRmLXRodW1ic1wvMTYwMTcuanBlZyIsImF1dG9PcGVuT3V0bGluZSI6ZmFsc2UsImF1dG9PcGVuVGh1bWJuYWlsIjpmYWxzZSwic2x1ZyI6IjE2MDE3IiwiaWQiOjE2MDE3LCJsaWdodGJveCI6InRodW1iIn0=  \">Formular Pr\u00e4diktive Diagnostik<\/div><script class=\"df-shortcode-script\" type=\"application\/javascript\">if(window.DEARPDF && window.DEARPDF.parseElements){window.DEARPDF.parseElements();}<\/script><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-22 fusion_builder_column_inner_1_1 1_1 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-text fusion-text-19 fusion-text-no-margin\" style=\"--awb-margin-bottom:0px;--awb-margin-left:10px;\"><p><a href=\"\/wp-content\/uploads\/2023\/03\/CeGaT_Formular_Praediktive_Diagnostik.pdf\" target=\"_blank\" rel=\"noopener\">Pr\u00e4diktive Diagnostik:<br \/>\n2. Probe herunterladen<\/a><\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-19 fusion_builder_column_1_4 1_4 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:50%;--awb-order-small:0;--awb-spacing-right-small:3.84%;--awb-spacing-left-small:3.84%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-23 fusion_builder_column_inner_1_1 1_1 fusion-flex-column fusion-flex-align-self-stretch fusion-animated\" style=\"--awb-overflow:hidden;--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:0px;--awb-spacing-left-small:0px;\" data-animationType=\"fadeInUp\" data-animationDuration=\"2.0\" data-animationOffset=\"top-into-view\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"df-element dvcss dvcss_e_eyJzb3VyY2UiOiJodHRwczpcL1wvY2VnYXQuY29tXC93cC1jb250ZW50XC91cGxvYWRzXC8yMDIzXC8xMVwvQ2VHYVRfQmVpc3BpZWxiZWZ1bmRfUmVwZWF0X0FuYWx5c2UucGRmIiwicGRmVGh1bWIiOiJodHRwczpcL1wvY2VnYXQuY29tXC93cC1jb250ZW50XC91cGxvYWRzXC9kZWFycGRmLXRodW1ic1wvNjE2ODYuanBlZyIsImF1dG9PcGVuT3V0bGluZSI6ZmFsc2UsImF1dG9PcGVuVGh1bWJuYWlsIjpmYWxzZSwic2x1ZyI6ImJlaXNwaWVsYmVmdW5kLXJlcGVhdC1hbmFseXNlIiwiaWQiOjYxNjg2LCJsaWdodGJveCI6InRodW1iIn0=  \">Beispielbefund Repeat Analyse<\/div><script class=\"df-shortcode-script\" type=\"application\/javascript\">if(window.DEARPDF && window.DEARPDF.parseElements){window.DEARPDF.parseElements();}<\/script><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-24 fusion_builder_column_inner_1_1 1_1 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-text fusion-text-20 fusion-text-no-margin\" style=\"--awb-margin-bottom:0px;--awb-margin-left:10px;\"><p><a href=\"\/wp-content\/uploads\/2023\/11\/CeGaT_Beispielbefund_Repeat_Analyse.pdf\" target=\"_blank\" rel=\"noopener\">Beispielbefund Repeat Analyse herunterladen<\/a><\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-20 fusion_builder_column_1_4 1_4 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:25%;--awb-margin-top-large:0px;--awb-spacing-right-large:7.68%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:7.68%;--awb-width-medium:25%;--awb-order-medium:0;--awb-spacing-right-medium:7.68%;--awb-spacing-left-medium:7.68%;--awb-width-small:50%;--awb-order-small:0;--awb-spacing-right-small:3.84%;--awb-spacing-left-small:3.84%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-25 fusion_builder_column_inner_1_1 1_1 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-overflow:hidden;--awb-bg-size:cover;--awb-border-color:var(--awb-color1);--awb-border-style:solid;--awb-border-radius:3px 3px 3px 3px;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-margin-bottom-medium:20px;--awb-spacing-left-medium:1.92%;--awb-width-small:50%;--awb-order-small:0;--awb-spacing-right-small:0px;--awb-spacing-left-small:0px;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"df-element dvcss dvcss_e_eyJzb3VyY2UiOiJcL3dwLWNvbnRlbnRcL3VwbG9hZHNcLzIwMjNcLzAzXC9DZUdhVF9TYW1wbGVfUmVwb3J0X1NlZ3JlZ2F0aW9uX0FuYWx5c2lzLnBkZiIsInBkZlRodW1iIjoiXC93cC1jb250ZW50XC91cGxvYWRzXC9kZWFycGRmLXRodW1ic1wvMTYwMTEuanBlZyIsImF1dG9PcGVuT3V0bGluZSI6ZmFsc2UsImF1dG9PcGVuVGh1bWJuYWlsIjpmYWxzZSwic2x1ZyI6IjE2MDExIiwiaWQiOjE2MDExLCJsaWdodGJveCI6InRodW1iIn0=  \">Sample Report Segregation Analysis<\/div><script class=\"df-shortcode-script\" type=\"application\/javascript\">if(window.DEARPDF && window.DEARPDF.parseElements){window.DEARPDF.parseElements();}<\/script><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-26 fusion_builder_column_inner_1_1 1_1 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-text fusion-text-21 fusion-text-no-margin\" style=\"--awb-margin-bottom:0px;--awb-margin-left:10px;\"><p><a href=\"\/wp-content\/uploads\/2023\/03\/CeGaT_Sample_Report_Segregation_Analysis.pdf\" target=\"_blank\" rel=\"noopener\">Beispielbefund Segregation Analyse (EN) herunterladen<\/a><\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><div id=\"kontakt-form\" class=\"fusion-container-anchor\"><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-11 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--awb-background-blend-mode:color;--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-padding-top:60px;--awb-padding-top-small:40px;--awb-margin-bottom:-60px;--awb-background-color:rgba(255,255,255,0.75);--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"max-width:1248px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-21 fusion_builder_column_1_2 1_2 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:50%;--awb-order-medium:0;--awb-spacing-right-medium:3.84%;--awb-spacing-left-medium:3.84%;--awb-width-small:100%;--awb-order-small:1;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-28 fusion-sep-none fusion-title-text fusion-title-size-two\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h2 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:36;line-height:var(--awb-typography1-line-height);\">Kontaktieren Sie uns<\/h2><\/div><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-27 fusion_builder_column_inner_1_1 1_1 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-margin-bottom-small:0px;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-text fusion-text-22\"><p style=\"text-align: justify;\">Sie haben noch eine Frage oder Interesse an unserem Service?<\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-28 fusion_builder_column_inner_1_1 1_1 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-form fusion-form-builder fusion-form-form-wrapper fusion-form-971\" style=\"--awb-tooltip-text-color:var(--awb-color6);--awb-tooltip-background-color:#333333;--awb-form-placeholder-color:var(--awb-color6);--awb-form-text-color:var(--awb-color6);--awb-form-focus-border-color:rgba(29,66,137,0.5);--awb-form-focus-border-hover-color:rgba(29,66,137,0.5);--awb-form-border-radius:3px;\" data-form-id=\"971\" data-config=\"{&quot;form_id&quot;:971,&quot;form_post_id&quot;:971,&quot;post_id&quot;:16019,&quot;form_type&quot;:&quot;ajax&quot;,&quot;confirmation_type&quot;:[&quot;redirect&quot;],&quot;redirect_url&quot;:&quot;https:\\\/\\\/cegat.com\\\/de\\\/danke\\\/&quot;,&quot;redirect_timeout&quot;:&quot;0&quot;,&quot;field_labels&quot;:{&quot;name&quot;:&quot;&quot;,&quot;email&quot;:&quot;&quot;,&quot;anfragender&quot;:&quot;&quot;,&quot;name_des_patienten&quot;:&quot;&quot;,&quot;country&quot;:&quot;&quot;,&quot;grund_der_kontaktaufnahme&quot;:&quot;&quot;,&quot;message&quot;:&quot;&quot;,&quot;datenschutz&quot;:&quot;&quot;},&quot;field_logics&quot;:{&quot;notice_1&quot;:&quot;&quot;,&quot;name&quot;:&quot;&quot;,&quot;email&quot;:&quot;&quot;,&quot;anfragender&quot;:&quot;&quot;,&quot;name_des_patienten&quot;:&quot;[{\\&quot;operator\\&quot;:\\&quot;or\\&quot;,\\&quot;comparison\\&quot;:\\&quot;contains\\&quot;,\\&quot;field\\&quot;:\\&quot;anfragender\\&quot;,\\&quot;value\\&quot;:\\&quot;\\u00c4rztin oder Arzt\\&quot;},{\\&quot;operator\\&quot;:\\&quot;and\\&quot;,\\&quot;comparison\\&quot;:\\&quot;contains\\&quot;,\\&quot;field\\&quot;:\\&quot;anfragender\\&quot;,\\&quot;value\\&quot;:\\&quot;Angeh\\u00f6rige oder Angeh\\u00f6riger einer Patientin oder eines Patienten\\&quot;}]&quot;,&quot;country&quot;:&quot;&quot;,&quot;grund_der_kontaktaufnahme&quot;:&quot;&quot;,&quot;message&quot;:&quot;&quot;,&quot;datenschutz&quot;:&quot;&quot;,&quot;submit_1&quot;:&quot;&quot;},&quot;field_types&quot;:{&quot;notice_1&quot;:&quot;notice&quot;,&quot;name&quot;:&quot;text&quot;,&quot;nachname&quot;:&quot;honeypot&quot;,&quot;email&quot;:&quot;email&quot;,&quot;anfragender&quot;:&quot;select&quot;,&quot;name_des_patienten&quot;:&quot;text&quot;,&quot;country&quot;:&quot;select&quot;,&quot;grund_der_kontaktaufnahme&quot;:&quot;select&quot;,&quot;message&quot;:&quot;textarea&quot;,&quot;datenschutz&quot;:&quot;consent&quot;,&quot;submit_1&quot;:&quot;submit&quot;,&quot;recaptcha_1&quot;:&quot;recaptcha&quot;},&quot;nonce_method&quot;:&quot;ajax&quot;,&quot;form_views&quot;:&quot;&quot;,&quot;form_views_counting&quot;:&quot;&quot;}\"><form action=\"https:\/\/cegat.com\/de\/diagnostik\/einzelgen-und-segregationsanalyse\/\" method=\"post\" class=\"fusion-form fusion-form-971\"><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-11-1 fusion-flex-container nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--link_hover_color: var(--awb-color1);--link_color: var(--awb-color6);--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-padding-top:0px;--awb-padding-right:0px;--awb-padding-bottom:0px;--awb-padding-left:0px;--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-22 fusion_builder_column_1_1 1_1 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-flex-grow:0;--awb-flex-shrink:0;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:10px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-flex-grow-medium:0;--awb-flex-shrink-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-flex-grow-small:0;--awb-flex-shrink-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"form-submission-notices data-notice_1\" id=\"fusion-notices-1\" data-instance=\"1\"><div class=\"fusion-alert alert success alert-success fusion-alert-center fusion-form-response fusion-form-response-success awb-alert-native-link-color alert-dismissable awb-alert-close-boxed\" role=\"alert\"><div class=\"fusion-alert-content-wrapper\"><span class=\"alert-icon\"><i class=\"awb-icon-check-circle\" aria-hidden=\"true\"><\/i><\/span><span class=\"fusion-alert-content\">Vielen Dank f\u00fcr Ihre Anfrage. Ihre Nachricht wurde versendet.<\/span><\/div><button type=\"button\" class=\"close toggle-alert\" data-dismiss=\"alert\" aria-label=\"Close\">&times;<\/button><\/div><div class=\"fusion-alert alert error alert-danger fusion-alert-center fusion-form-response fusion-form-response-error awb-alert-native-link-color alert-dismissable awb-alert-close-boxed\" role=\"alert\"><div class=\"fusion-alert-content-wrapper\"><span class=\"alert-icon\"><i class=\"awb-icon-exclamation-triangle\" aria-hidden=\"true\"><\/i><\/span><span class=\"fusion-alert-content\">Leider ist ein Fehler beim versenden aufgetreten. Bitte versuchen Sie es zu einem sp\u00e4teren Zeitpunkt noch einmal oder informieren Sie uns per sales@cegat.de<\/span><\/div><button type=\"button\" class=\"close toggle-alert\" data-dismiss=\"alert\" aria-label=\"Close\">&times;<\/button><\/div><\/div><div class=\"fusion-form-field fusion-form-text-field fusion-form-label-above\" style=\"\" data-form-id=\"971\"><input type=\"text\" autocomplete=\"off\"  data-invalid-notice=\"Die Angabe ist leider fehlerhaft.\"  data-empty-notice=\"Bitte tragen Sie hier Ihren Namen ein.\" name=\"name\" id=\"name\" value=\"\"  class=\"fusion-form-input\" required=\"true\" aria-required=\"true\" placeholder=\"Name *\" data-holds-private-data=\"false\" minlength=\"0\"\/><\/div><div class=\"fusion-form-field fusion-form-honeypot-field fusion-form-label-above\" style=\"\" data-form-id=\"971\"><input type=\"hidden\" tabindex=\"-1\" name=\"nachname\" class=\"fusion-form-input\" autocomplete=\"hypot-69efb5366ab30\" aria-hidden=\"true\" data-fusion-is-honeypot=\"true\"><\/div><div class=\"fusion-form-field fusion-form-email-field fusion-form-label-above\" style=\"\" data-form-id=\"971\"><input type=\"email\" autocomplete=\"off\"  data-empty-notice=\"Bitte tragen Sie hier Ihren E-Mail-Adresse ein.\" name=\"email\" id=\"email\" value=\"\"  class=\"fusion-form-input\" required=\"true\" aria-required=\"true\" placeholder=\"E-Mail *\" data-holds-private-data=\"false\"\/><\/div><div class=\"fusion-form-field fusion-form-select-field fusion-form-label-above\" style=\"\" data-form-id=\"971\"><div class=\"fusion-select-wrapper\"><select autocomplete=\"off\" data-empty-notice=\"Bitte w\u00e4hlen Sie eine Option.\" tabindex=\"\" id=\"anfragender\" name=\"anfragender\" class=\"fusion-form-input\" required=\"true\" aria-required=\"true\" data-holds-private-data=\"false\"><option value=\"\" disabled selected>Anfragende oder Anfragender *<\/option><option value=\"\u00c4rztin oder Arzt\" >\u00c4rztin oder Arzt<\/option><option value=\"Patientin oder Patient\" >Patientin oder Patient<\/option><option value=\"Angeh\u00f6rige oder Angeh\u00f6riger einer Patientin oder eines Patienten\" >Angeh\u00f6rige oder Angeh\u00f6riger einer Patientin oder eines Patienten<\/option><option value=\"Mitarbeiterin oder Mitarbeiter Forschung\/Universit\u00e4t\" >Mitarbeiterin oder Mitarbeiter Forschung\/Universit\u00e4t<\/option><option value=\"Sonstiges\" >Sonstiges<\/option><\/select><div class=\"select-arrow\"><svg width=\"12\" height=\"8\" viewBox=\"0 0 12 8\" fill=\"none\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\"> <path d=\"M1.5 1.75L6 6.25L10.5 1.75\" stroke=\"#6D6D6D\" stroke-width=\"2\" stroke-linecap=\"round\" stroke-linejoin=\"round\"\/> <\/svg><\/div><\/div><\/div><div class=\"fusion-form-field fusion-form-text-field fusion-form-label-above fusion-form-field-hidden\" style=\"\" data-form-id=\"971\" data-form-element-name=\"text_2\"><input type=\"text\" autocomplete=\"off\" name=\"name_des_patienten\" id=\"name_des_patienten\" value=\"\"  class=\"fusion-form-input\" placeholder=\"Name der Patientin oder des Patienten \" data-holds-private-data=\"false\" minlength=\"0\"\/><\/div><div class=\"fusion-form-field fusion-form-select-field fusion-form-label-above\" style=\"\" data-form-id=\"971\"><div class=\"fusion-select-wrapper\"><select autocomplete=\"off\" data-empty-notice=\"Bitte w\u00e4hlen Sie ein Land.\" tabindex=\"\" id=\"country\" name=\"country\" class=\"fusion-form-input\" required=\"true\" aria-required=\"true\" data-holds-private-data=\"false\"><option value=\"\" disabled selected>Land des Wohnsitz der Patientin oder des Patienten*<\/option><option value=\"Afghanistan\" >Afghanistan<\/option><option value=\"\u00c4gypten\" >\u00c4gypten<\/option><option value=\"Albanien\" >Albanien<\/option><option value=\"Algerien\" >Algerien<\/option><option value=\"Andorra\" >Andorra<\/option><option value=\"Anguilla\" >Anguilla<\/option><option value=\"\u00c4quatorialguinea\" >\u00c4quatorialguinea<\/option><option value=\"Argentinien\" >Argentinien<\/option><option value=\"Armenien\" >Armenien<\/option><option value=\"Aruba\" >Aruba<\/option><option value=\"Ascension und Tris\" >Ascension und Tris<\/option><option value=\"Aserbaidschan\" >Aserbaidschan<\/option><option value=\"Australien\" >Australien<\/option><option value=\"Bahamas\" >Bahamas<\/option><option value=\"Bahrain\" >Bahrain<\/option><option value=\"Bangladesch\" >Bangladesch<\/option><option value=\"Barbados\" >Barbados<\/option><option value=\"Belarus\" >Belarus<\/option><option value=\"Belgien\" >Belgien<\/option><option value=\"Belize\" >Belize<\/option><option value=\"Benin\" >Benin<\/option><option value=\"Bhutan\" >Bhutan<\/option><option value=\"Bolivien\" >Bolivien<\/option><option value=\"Bonaire\" >Bonaire<\/option><option value=\"Bosnien und Herzegowina (Republika Srpska)\" >Bosnien und Herzegowina (Republika Srpska)<\/option><option value=\"Bosnien und Herzegowina (F\u00f6deration Bosnien und Herzegowina)\" >Bosnien und Herzegowina (F\u00f6deration Bosnien und Herzegowina)<\/option><option value=\"Botswana\" >Botswana<\/option><option value=\"Bouvet\" >Bouvet<\/option><option value=\"Brasilien\" >Brasilien<\/option><option value=\"Britische Jungferninseln\" >Britische Jungferninseln<\/option><option value=\"Brunei\" >Brunei<\/option><option value=\"Bulgarien\" >Bulgarien<\/option><option value=\"Burkina Faso\" >Burkina Faso<\/option><option value=\"Burundi\" >Burundi<\/option><option value=\"Chile\" >Chile<\/option><option value=\"China\" >China<\/option><option value=\"Costa Rica\" >Costa Rica<\/option><option value=\"Cura\u00e7ao\" >Cura\u00e7ao<\/option><option value=\"D\u00e4nemark\" >D\u00e4nemark<\/option><option value=\"Deutschland\" >Deutschland<\/option><option value=\"Dominica\" >Dominica<\/option><option value=\"Dominikanische Republik\" >Dominikanische Republik<\/option><option value=\"Dschibuti\" >Dschibuti<\/option><option value=\"Ecuador\" >Ecuador<\/option><option value=\"El Salvador\" >El Salvador<\/option><option value=\"Elfenbeink\u00fcste\" >Elfenbeink\u00fcste<\/option><option value=\"Eritrea\" >Eritrea<\/option><option value=\"Estland\" >Estland<\/option><option value=\"Falklandinseln\" >Falklandinseln<\/option><option value=\"F\u00e4r\u00f6er\" >F\u00e4r\u00f6er<\/option><option value=\"Fidschi\" >Fidschi<\/option><option value=\"Finnland\" >Finnland<\/option><option value=\"Frankreich\" >Frankreich<\/option><option value=\"Gabun\" >Gabun<\/option><option value=\"Gambia\" >Gambia<\/option><option value=\"Georgien\" >Georgien<\/option><option value=\"Ghana\" >Ghana<\/option><option value=\"Gibraltar\" >Gibraltar<\/option><option value=\"Grenada\" >Grenada<\/option><option value=\"Griechenland\" >Griechenland<\/option><option value=\"Gr\u00f6nland\" >Gr\u00f6nland<\/option><option value=\"Gro\u00dfbritannien\" >Gro\u00dfbritannien<\/option><option value=\"Guadeloupe\" >Guadeloupe<\/option><option value=\"Guam\" >Guam<\/option><option value=\"Guatemala\" >Guatemala<\/option><option value=\"Guernsey\" >Guernsey<\/option><option value=\"Guinea\" >Guinea<\/option><option value=\"Guinea-Bissau\" >Guinea-Bissau<\/option><option value=\"Guyana\" >Guyana<\/option><option value=\"Haiti\" >Haiti<\/option><option value=\"Honduras\" >Honduras<\/option><option value=\"Hongkong\" >Hongkong<\/option><option value=\"Indien\" >Indien<\/option><option value=\"Indonesien\" >Indonesien<\/option><option value=\"Irak\" >Irak<\/option><option value=\"Iran\" >Iran<\/option><option value=\"Irland\" >Irland<\/option><option value=\"Island\" >Island<\/option><option value=\"Isle of Man\" >Isle of Man<\/option><option value=\"Israel\" >Israel<\/option><option value=\"Italien\" >Italien<\/option><option value=\"Jamaika\" >Jamaika<\/option><option value=\"Japan\" >Japan<\/option><option value=\"Jemen\" >Jemen<\/option><option value=\"Jersey\" >Jersey<\/option><option value=\"Jordanien\" >Jordanien<\/option><option value=\"Kaimaninseln\" >Kaimaninseln<\/option><option value=\"Kambodscha\" >Kambodscha<\/option><option value=\"Kamerun\" >Kamerun<\/option><option value=\"Kanada\" >Kanada<\/option><option value=\"Kap Verde\" >Kap Verde<\/option><option value=\"Kasachstan\" >Kasachstan<\/option><option value=\"Katar\" >Katar<\/option><option value=\"Kenia\" >Kenia<\/option><option value=\"Kirgisistan\" >Kirgisistan<\/option><option value=\"Kiribati\" >Kiribati<\/option><option value=\"Kolumbien\" >Kolumbien<\/option><option value=\"Komoren\" >Komoren<\/option><option value=\"Kongo Brazzaville\" >Kongo Brazzaville<\/option><option value=\"Kongo-Kinshasa\" >Kongo-Kinshasa<\/option><option value=\"Kosovo\" >Kosovo<\/option><option value=\"Kroatien\" >Kroatien<\/option><option value=\"Kuba\" >Kuba<\/option><option value=\"Kuwait\" >Kuwait<\/option><option value=\"Laos\" >Laos<\/option><option value=\"Lesotho\" >Lesotho<\/option><option value=\"Lettland\" >Lettland<\/option><option value=\"Libanon\" >Libanon<\/option><option value=\"Liberia\" >Liberia<\/option><option value=\"Libyen\" >Libyen<\/option><option value=\"Liechtenstein\" >Liechtenstein<\/option><option value=\"Litauen\" >Litauen<\/option><option value=\"Luxemburg\" >Luxemburg<\/option><option value=\"Macau\" >Macau<\/option><option value=\"Madagaskar\" >Madagaskar<\/option><option value=\"Malawi\" >Malawi<\/option><option value=\"Malaysia\" >Malaysia<\/option><option value=\"Malediven\" >Malediven<\/option><option value=\"Mali\" >Mali<\/option><option value=\"Malta\" >Malta<\/option><option value=\"Marokko\" >Marokko<\/option><option value=\"Marshallinseln\" >Marshallinseln<\/option><option value=\"Martinique\" >Martinique<\/option><option value=\"Mauretanien\" >Mauretanien<\/option><option value=\"Mauritius\" >Mauritius<\/option><option value=\"Mayotte\" >Mayotte<\/option><option value=\"Mexiko\" >Mexiko<\/option><option value=\"Mikronesien\" >Mikronesien<\/option><option value=\"Moldawien\" >Moldawien<\/option><option value=\"Monaco\" >Monaco<\/option><option value=\"Mongolei\" >Mongolei<\/option><option value=\"Montenegro\" >Montenegro<\/option><option value=\"Montserrat\" >Montserrat<\/option><option value=\"Mosambik\" >Mosambik<\/option><option value=\"Myanmar\" >Myanmar<\/option><option value=\"Namibia\" >Namibia<\/option><option value=\"Nauru\" >Nauru<\/option><option value=\"Nepal\" >Nepal<\/option><option value=\"Neuseeland\" >Neuseeland<\/option><option value=\"Nicaragua\" >Nicaragua<\/option><option value=\"Niederlande\" >Niederlande<\/option><option value=\"Niger\" >Niger<\/option><option value=\"Nigeria\" >Nigeria<\/option><option value=\"Nordkorea\" >Nordkorea<\/option><option value=\"Nordmazedonien\" >Nordmazedonien<\/option><option value=\"Norfolk\" >Norfolk<\/option><option value=\"Norwegen\" >Norwegen<\/option><option value=\"Oman\" >Oman<\/option><option value=\"\u00d6sterreich\" >\u00d6sterreich<\/option><option value=\"Osttimor\" >Osttimor<\/option><option value=\"Pakistan\" >Pakistan<\/option><option value=\"Pal\u00e4stinensische Autonomiebeh\u00f6rde\" >Pal\u00e4stinensische Autonomiebeh\u00f6rde<\/option><option value=\"Palau\" >Palau<\/option><option value=\"Panama\" >Panama<\/option><option value=\"Papua-Neuguinea\" >Papua-Neuguinea<\/option><option value=\"Paraguay\" >Paraguay<\/option><option value=\"Peru\" >Peru<\/option><option value=\"Philippinen\" >Philippinen<\/option><option value=\"Pitcairninseln\" >Pitcairninseln<\/option><option value=\"Polen\" >Polen<\/option><option value=\"Portugal\" >Portugal<\/option><option value=\"Puerto Rico\" >Puerto Rico<\/option><option value=\"Ruanda\" >Ruanda<\/option><option value=\"Rum\u00e4nien\" >Rum\u00e4nien<\/option><option value=\"Russland\" >Russland<\/option><option value=\"Saint-Barth\u00e9lemy\" >Saint-Barth\u00e9lemy<\/option><option value=\"Saint-Pierre und Miquelon\" >Saint-Pierre und Miquelon<\/option><option value=\"Salomonen\" >Salomonen<\/option><option value=\"Sambia\" >Sambia<\/option><option value=\"Samoa\" >Samoa<\/option><option value=\"San Marino\" >San Marino<\/option><option value=\"S\u00e3o Tom\u00e9 und Pr\u00edncipe\" >S\u00e3o Tom\u00e9 und Pr\u00edncipe<\/option><option value=\"Saudi-Arabien\" >Saudi-Arabien<\/option><option value=\"Schweden\" >Schweden<\/option><option value=\"Schweiz\" >Schweiz<\/option><option value=\"Senegal\" >Senegal<\/option><option value=\"Serbien\" >Serbien<\/option><option value=\"Seychellen\" >Seychellen<\/option><option value=\"Sierra Leone\" >Sierra Leone<\/option><option value=\"Simbabwe\" >Simbabwe<\/option><option value=\"Singapur\" >Singapur<\/option><option value=\"Sint Eustatius und Saba\" >Sint Eustatius und Saba<\/option><option value=\"Slowakei\" >Slowakei<\/option><option value=\"Slowenien\" >Slowenien<\/option><option value=\"Somalia\" >Somalia<\/option><option value=\"Spanien\" >Spanien<\/option><option value=\"Sri Lanka\" >Sri Lanka<\/option><option value=\"St. Helena\" >St. Helena<\/option><option value=\"St. Kitts und Nevis\" >St. Kitts und Nevis<\/option><option value=\"St. Lucia\" >St. Lucia<\/option><option value=\"St. Martin\" >St. Martin<\/option><option value=\"St. Vincent und die Grenadinen\" >St. Vincent und die Grenadinen<\/option><option value=\"S\u00fcdafrika\" >S\u00fcdafrika<\/option><option value=\"Sudan\" >Sudan<\/option><option value=\"S\u00fcdgeorgien und die S\u00fcdliche Antarktisinseln\" >S\u00fcdgeorgien und die S\u00fcdliche Antarktisinseln<\/option><option value=\"S\u00fcdkorea\" >S\u00fcdkorea<\/option><option value=\"Suriname\" >Suriname<\/option><option value=\"Swasiland\" >Swasiland<\/option><option value=\"Syrien\" >Syrien<\/option><option value=\"Tadschikistan\" >Tadschikistan<\/option><option value=\"Taiwan\" >Taiwan<\/option><option value=\"Tansania\" >Tansania<\/option><option value=\"Thailand\" >Thailand<\/option><option value=\"Togo\" >Togo<\/option><option value=\"Tokelau-Inseln\" >Tokelau-Inseln<\/option><option value=\"Tonga\" >Tonga<\/option><option value=\"Trinidad und Tobago\" >Trinidad und Tobago<\/option><option value=\"Tschad\" >Tschad<\/option><option value=\"Tschechische Republik\" >Tschechische Republik<\/option><option value=\"Tunesien\" >Tunesien<\/option><option value=\"T\u00fcrkei\" >T\u00fcrkei<\/option><option value=\"Turkmenistan\" >Turkmenistan<\/option><option value=\"Turks- und Caicosinseln\" >Turks- und Caicosinseln<\/option><option value=\"Tuvalu\" >Tuvalu<\/option><option value=\"Uganda\" >Uganda<\/option><option value=\"Ukraine\" >Ukraine<\/option><option value=\"Ungarn\" >Ungarn<\/option><option value=\"Uruguay\" >Uruguay<\/option><option value=\"Usbekistan\" >Usbekistan<\/option><option value=\"Vanuatu\" >Vanuatu<\/option><option value=\"Vatikanstadt\" >Vatikanstadt<\/option><option value=\"Venezuela\" >Venezuela<\/option><option value=\"Vereinigte Arabische Emirate\" >Vereinigte Arabische Emirate<\/option><option value=\"Vereinigte Staaten\" >Vereinigte Staaten<\/option><option value=\"Vereinigtes K\u00f6nigreich\" >Vereinigtes K\u00f6nigreich<\/option><option value=\"Vietnam\" >Vietnam<\/option><option value=\"Westsahara\" >Westsahara<\/option><option value=\"Zentralafrikanische Republik\" >Zentralafrikanische Republik<\/option><option value=\"Zypern\" >Zypern<\/option><\/select><div class=\"select-arrow\"><svg width=\"12\" height=\"8\" viewBox=\"0 0 12 8\" fill=\"none\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\"> <path d=\"M1.5 1.75L6 6.25L10.5 1.75\" stroke=\"#6D6D6D\" stroke-width=\"2\" stroke-linecap=\"round\" stroke-linejoin=\"round\"\/> <\/svg><\/div><\/div><\/div><div class=\"fusion-form-field fusion-form-select-field fusion-form-label-above\" style=\"\" data-form-id=\"971\"><div class=\"fusion-select-wrapper\"><select autocomplete=\"off\" data-empty-notice=\"Bitte w\u00e4hlen Sie eine Option.\" tabindex=\"\" id=\"grund_der_kontaktaufnahme\" name=\"grund_der_kontaktaufnahme\" class=\"fusion-form-input\" required=\"true\" aria-required=\"true\" data-holds-private-data=\"false\"><option value=\"\" disabled selected>Grund der Kontaktaufnahme *<\/option><option value=\"Diagnostik einer seltenen Erkrankung\" >Diagnostik einer seltenen Erkrankung<\/option><option value=\"Tumorerkrankung\" >Tumorerkrankung<\/option><option value=\"Gesundheitsvorsorge\" >Gesundheitsvorsorge<\/option><option value=\"Familienplanung\" >Familienplanung<\/option><option value=\"Sequenzierdienstleistungen (ohne Befund)\" >Sequenzierdienstleistungen (ohne Befund)<\/option><option value=\"Sonstiges\" >Sonstiges<\/option><\/select><div class=\"select-arrow\"><svg width=\"12\" height=\"8\" viewBox=\"0 0 12 8\" fill=\"none\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\"> <path d=\"M1.5 1.75L6 6.25L10.5 1.75\" stroke=\"#6D6D6D\" stroke-width=\"2\" stroke-linecap=\"round\" stroke-linejoin=\"round\"\/> <\/svg><\/div><\/div><\/div><div class=\"fusion-form-field fusion-form-textarea-field fusion-form-label-above\" style=\"\" data-form-id=\"971\"><textarea cols=\"40\" autocomplete=\"off\"  minlength=\"0\"  rows=\"5\" tabindex=\"\" id=\"message\" name=\"message\" class=\"fusion-form-input\" required=\"true\" aria-required=\"true\" placeholder=\"Informationen zur Patientin oder zum Patienten (Verdachtsdiagnose\/Anamnese) *\" data-holds-private-data=\"false\"><\/textarea><\/div><div class=\"fusion-form-field fusion-form-consent-field fusion-form-label-above\" style=\"\" data-form-id=\"971\"><p class=\"label\">Mit Klick auf den \"Absenden\" Button stimme ich der Daten\u00fcbertragung an CeGaT zu.<\/p><input name=\"datenschutz\" type=\"hidden\" value=\"1\"\/><\/div><div class=\"fusion-form-field fusion-form-submit-field fusion-form-label-above\" style=\"\" data-form-id=\"971\"><div ><button type=\"submit\" class=\"fusion-button button-flat fusion-button-default-size button-custom fusion-button-default button-7 fusion-button-default-span  button-default form-form-submit\" style=\"--awb-padding-right:50px;--awb-padding-left:50px;--button_accent_color:var(--awb-color1);--button_border_color:var(--awb-color1);--button_accent_hover_color:var(--awb-color5);--button_border_hover_color:rgba(255,255,255,0);--button_border_width-top:1px;--button_border_width-right:1px;--button_border_width-bottom:1px;--button_border_width-left:1px;--button_gradient_top_color:rgba(29,66,137,0);--button_gradient_bottom_color:rgba(29,66,137,0);--button_gradient_top_color_hover:var(--awb-color1);--button_gradient_bottom_color_hover:var(--awb-color1);\" data-form-number=\"971\" tabindex=\"\"><span class=\"fusion-button-text awb-button__text awb-button__text--default\">Absenden<\/span><\/button><\/div><\/div><div class=\"fusion-form-field fusion-form-recaptcha-field fusion-form-label-above\" style=\"\" data-form-id=\"971\">\t\t\t\t<div class=\"form-creator-recaptcha\" >\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<div class=\"fusion-form-recaptcha-wrapper\">\n\t\t\t\t\t\t\t\t\t\t<div\n\t\t\t\t\t\t\tid=\"g-recaptcha-id-form-971\"\n\t\t\t\t\t\t\tclass=\"fusion-form-recaptcha-v3 recaptcha-container \"\n\t\t\t\t\t\t\tdata-sitekey=\"6Leoiq0kAAAAAAUdYtm1y6hwvajFVKUTHngOajYi\"\n\t\t\t\t\t\t\tdata-badge=\"inline\">\n\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<input\n\t\t\t\t\t\t\ttype=\"hidden\"\n\t\t\t\t\t\t\tname=\"fusion-form-recaptcha-response\"\n\t\t\t\t\t\t\tclass=\"g-recaptcha-response\"\n\t\t\t\t\t\t\tid=\"fusion-form-recaptcha-response-971\"\n\t\t\t\t\t\t\tvalue=\"\">\n\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div><div class=\"fusion-text fusion-text-23\" style=\"--awb-font-size:14px;--awb-text-color:var(--awb-custom_color_1);\"><p>Mit (*) gekennzeichnete Felder sind Pflichtfelder und m\u00fcssen ausgef\u00fcllt werden.<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div><input type=\"hidden\" name=\"fusion_privacy_expiration_interval\" value=\"3\"><input type=\"hidden\" name=\"privacy_expiration_action\" value=\"delete\"><\/form><\/div><\/div><\/div><\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-23 fusion_builder_column_1_2 1_2 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:50%;--awb-flex-grow:0;--awb-flex-shrink:0;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:50%;--awb-order-medium:0;--awb-flex-grow-medium:0;--awb-flex-shrink-medium:0;--awb-spacing-right-medium:3.84%;--awb-spacing-left-medium:3.84%;--awb-width-small:100%;--awb-order-small:3;--awb-flex-grow-small:0;--awb-flex-shrink-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-title title fusion-title-29 fusion-sep-none fusion-title-text fusion-title-size-two\" style=\"--awb-text-color:var(--awb-color1);--awb-margin-top-small:10px;--awb-margin-right-small:0px;--awb-margin-bottom-small:10px;--awb-margin-left-small:0px;\"><h2 class=\"fusion-title-heading title-heading-left fusion-responsive-typography-calculated\" style=\"margin:0;text-transform:none;--fontSize:36;line-height:var(--awb-typography1-line-height);\">Diagnostik-Support<\/h2><\/div><div class=\"fusion-builder-row fusion-builder-row-inner fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"--awb-flex-grow:0;--awb-flex-grow-medium:0;--awb-flex-grow-small:0;--awb-flex-shrink:0;--awb-flex-shrink-medium:0;--awb-flex-shrink-small:0;width:104% !important;max-width:104% !important;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-29 fusion_builder_column_inner_1_1 1_1 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-text fusion-text-24\"><p style=\"text-align: justify;\">Wir unterst\u00fctzen Sie auf Wunsch bei der Auswahl der diagnostischen Strategie \u2013 f\u00fcr jede einzelne Patientin und jeden einzelnen Patienten.<\/p>\n<\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column_inner fusion-builder-nested-column-30 fusion_builder_column_inner_1_1 1_1 fusion-flex-column fusion-flex-align-self-stretch\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:10px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element \" style=\"--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-14 hover-type-none\" style=\"border-radius:3px;\"><img decoding=\"async\" width=\"600\" height=\"400\" alt=\"Keimbahn Team der CeGaT\" title=\"CeGaT_internal_Germline-Team\" src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/11\/CeGaT_internal_Germline-Team.jpg\" data-orig-src=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/11\/CeGaT_internal_Germline-Team.jpg\" class=\"lazyload img-responsive wp-image-62100\" srcset=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27600%27%20height%3D%27400%27%20viewBox%3D%270%200%20600%20400%27%3E%3Crect%20width%3D%27600%27%20height%3D%27400%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-srcset=\"https:\/\/cegat.com\/wp-content\/uploads\/2023\/11\/CeGaT_internal_Germline-Team-200x133.jpg 200w, https:\/\/cegat.com\/wp-content\/uploads\/2023\/11\/CeGaT_internal_Germline-Team-400x267.jpg 400w, https:\/\/cegat.com\/wp-content\/uploads\/2023\/11\/CeGaT_internal_Germline-Team.jpg 600w\" data-sizes=\"auto\" data-orig-sizes=\"(max-width: 768px) 100vw, 600px\" \/><\/span><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>\n<\/p>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":18,"featured_media":0,"parent":1779,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"100-width.php","meta":{"footnotes":""},"class_list":["post-16019","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Einzelgen- und Segregationsanalyse<\/title>\n<meta name=\"description\" content=\"&gt; 700 verschiedene Einzelgen-Sequenzanalysen. 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