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  2. Coagulopathies (2 genes)

Coagulopathies (2 genes)

Genetic test Export to PDF
Full name:
Coagulopathies (2 genes)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Post-natal Diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Amniotic fluid,
Chorionic villi,
DNA
Method category:
Sequence analysis: entire coding region
Deletion/duplication analysis
Method technique:
Next Generation Sequencing (NGS)
MLPA based techniques
Bi-directional Sanger Sequence analysis
Laboratory:
Centre de Génétique Médicale UCL
RIZIV code:
565471-565482
Turnaround time (maximum):
3 months
Document(s):
Created:
24 Jul 2019 - 16:22
Changed:
14 Dec 2023 - 15:12