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Caption : Accreditation =Accreditation
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NETHERLANDS

Limburg
MAASTRICHT

Accreditation
Molecular diagnosis of Congenital Heart Defects (NKX2-5, GATA4, TBX5, CRELD1, NOTCH1, TBX20, ACVR2B, CFC1, ZIC3, NODAL and JAG1 gene)
AZM - Academisch Ziekenhuis Maastricht
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SWITZERLAND

Suisse Alémanique
SCHLIEREN

Molecular diagnosis of mitral valve prolapse
Center for Cardiovascular Genetics and Gene Diagnostics
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

AQUITAINE
BORDEAUX

Diagnosis of periventricular nodular heterotopia (Panel)
CHU de Bordeaux-GH Pellegrin
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technical procedure(s) : NGS sequencing (except WES)

FRANCE

RHONE-ALPES
BRON

Diagnosis of congenital heart malformations (Panel)
CHU de Lyon HCL - GH Est
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Deletion / Duplication analysis
Technical procedure(s) : NGS sequencing (except WES)