Craniosynostosis / Crouzon syndrome (hot spot mutation - exon 9)

Genetic test Export to PDF
Full name:
Craniosynostosis / Crouzon syndrome (hot spot mutation - exon 9)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Amniotic fluid,
Chorionic villi,
DNA
Method category:
Method technique:
Laboratory:
RIZIV code:
EQA:
  • 2020 Skeletal dysplasis GenQA (Genomics Quality Assessment)
Turnaround time (maximum):
21 days
Document(s):
Created:
20 Aug 2019 - 12:05
Changed:
16 Jan 2024 - 13:20
URL: