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  2. Hemophilia B

Hemophilia B

This test requires filling out a specific Application Form available in the "document" field

Genetic test Export to PDF
Full name:
Hemophilia B
Description:

Screening of all coding exons of the F9 gene.
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
Method category:
Sequence analysis: entire coding region
Deletion/duplication analysis
Method technique:
Next Generation Sequencing (NGS)
MLPA based techniques
Laboratory:
Centrum Menselijke Erfelijkheid - KUL
RIZIV code:
565471-565482
Turnaround time (maximum):
3 - 4 months
Document(s):
Created:
19 Jul 2019 - 12:32
Changed:
14 Dec 2021 - 11:16
URL:
https://laboboeken.nexuzhealth.com/pboek/internet/GHB%20CME/14756