Craniosynostosis syndromes (Apert, Crouzon)

Genetic test Export to PDF
Full name:
Craniosynostosis syndromes (Apert, Crouzon)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Method technique:
Laboratory:
RIZIV code:
Turnaround time (maximum):
2 months
Document(s):
Created:
20 Aug 2019 - 12:05
Changed:
21 Jun 2022 - 12:25
URL: