Search for a diagnostic test
6 Result(s)
Caption
: Accreditation
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GERMANY
Bayern
MÜNCHEN
Molecular diagnosis of Brain Malformations / Neuronal Migration Disorders (NGS screening panel, 269 genes)
Medizinisch Genetisches Zentrum München
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing

SPAIN
Cataluña
L'HOSPITALET DE LLOBREGAT
Diagnosis of Sturge-Weber syndrome (GNAQ gene)
Reference Laboratory Genetics
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

PORTUGAL
NORTE
PORTO
Molecular diagnosis of Sturge-Weber syndrome (GNAQ gene: targeted mutation analysis, p.Arg183Gln
CGC Genetics / Centro de Genética Clínica
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis

AUSTRIA
WIEN
WIEN
Molecular diagnosis of Sturge-Weber syndrome (GNAQ gene)
Medizinische Universität Wien
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

FRANCE
BOURGOGNE-FRANCHE-COMTE
DIJON
Diagnosis of a mosaic development anomaly (AKT1, AKT3, GNA11, GNAQ, HRAS, KRAS, MTOR, NRAS, BRAF, PIK3CA, PIK3R2, TEK, FGFR1, FGFR2, FGFR3, KRT1, KRT10 genes)
CHU de Dijon - Plateau technique de Biologie
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

SPAIN
Madrid
SAN SEBASTIÁN DE LOS REYES