1. Genetic tests
  2. Beta-globin hemoglobinopathies

Beta-globin hemoglobinopathies

Genetic test Export to PDF
Full name:
Beta-globin hemoglobinopathies
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
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:
Bi-directional Sanger Sequence analysis
MLPA based techniques
Laboratory:
Centre de Génétique Médicale UCL
RIZIV code:
565471-565482
EQA:
  • 2015 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2016 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2017 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2018 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2019 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2022 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2023 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
Turnaround time (maximum):
2 months
Document(s):
Created:
24 Jul 2019 - 11:39
Changed:
19 Jan 2024 - 11:31