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Products found: 47Search results

University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale

Disorder Genes Test Method Lab Info Product code  
University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale Achondroplasia FGFR3, Sequence analysis of select exons
University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale Alpha1-Antitrypsin Deficiency SERPINA1, Targeted mutation analysis
University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale Angelman Syndrome UBE3A, Methylation analysis
University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy 9 Sequence analysis of the entire coding region
University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale ARX-Related Disorders ARX, Sequence analysis of the entire coding region
University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale Brugada Syndrome 1 SCN5A, Sequence analysis of the entire coding region
University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale CASQ2-Related Catecholaminergic Polymorphic Ventricular Tachycardia CASQ2, Sequence analysis of the entire coding region
University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale CFTR-Related Disorders CFTR, Targeted mutation analysis
University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale Charcot-Marie-Tooth Neuropathy Type 1E Sequence analysis of the entire coding region
University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale Charcot-Marie-Tooth Neuropathy X Type 1 GJB1, Sequence analysis of the entire coding region
University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale Early-Onset Primary Dystonia (DYT1) TOR1A, Sequence analysis of the entire coding region
University Hospital Lausanne, DNA Diagnostic Laboratory - Service de Génétique Médicale Fabry Disease GLA, Sequence analysis of the entire coding region
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