1. Genetic tests
  2. Hemophilia B

Hemophilia B

Genetic test Export to PDF
Full name:
Hemophilia B
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Mutation confirmation,
Post-natal Diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Chorionic villi,
Amniotic fluid,
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
EQA:
  • 2019 Genetics of heritable Bleeding Disorders UK NEQAS For Blood Coagulation
  • 2022 Genetics of heritable Bleeding Disorders UK NEQAS For Blood Coagulation
Accreditation (ISO 15189):
2022-12-22 / 2027-12-21
Turnaround time (maximum):
3 months
Document(s):
Created:
19 Jul 2019 - 12:32
Changed:
14 Dec 2023 - 15:24