Family Planning Panel Panel for Fertility
Prenatal ExomeXtra® Prenatal Array CGH Prenatal Single Gene & Segregation Analysis Harmony® Test Rhesus-NIPT
Exome Diagnostics Blood Disorders Cardiac Diseases Ciliopathies Connective Tissue Diseases Epilepsy & Brain Development Disorders Eye Diseases Fertility Hearing Loss Immune Disorders Kidney Diseases Liver Diseases Metabolic Diseases incl. Mitochondriopathies Neurodegenerative Diseases Neuromuscular Diseases Skeletal Disorders Skin Diseases
Hereditary Tumor Syndromes Molecular Pathology Comprehensive Tumor Diagnostics RNA-based Fusion Detection Tumor Exome & Transcriptome Neoantigen Identification Monitoring Tumor Therapy Recommendation
Exome Diagnostics Panel Diagnostics Array CGH Single Gene & Segregation Analysis
CeGaT’s Diagnostic Advantages Pedigree Creation Order Forms & Downloads Notes for Sample Requirements Diagnostic Support myCeGaT Portal – Infos & FAQ
Genome SequencingExomeXtra® SequencingExome SequencingTranscriptome SequencingPanel SequencingReady to Load SequencingSingle-Cell RNA SequencingSmall RNA Sequencing
Methylation Sequencing
Shotgun Metagenomic Sequencing Full-Length 16S Sequencing
Comprehensive Tumor Profiling Liquid Biopsy TSO500
HLA Typing T-Cell Receptor Sequencing Single-Cell Immune Profiling
Clinical Study Services
Sample Requirements Sequencing Technologies FAQs Downloads
News Publications
Press Releases
January 01, 2015
Pera J, Lechner S, Biskup S, Strach M, Grodzicki T, Slowik A.
No abstract available
View this paper on NCBI
