1. Genetic tests
  2. Beta-globin hemoglobinopathies (full sequencing)

Beta-globin hemoglobinopathies (full sequencing)

Genetic test Export to PDF
Full name:
Beta-globin hemoglobinopathies (full sequencing)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Chorionic villi,
Amniotic fluid,
Dried blood spot card
Method category:
Sequence analysis: entire coding region
Deletion/duplication analysis
Method technique:
Bi-directional Sanger Sequence analysis
MLPA based techniques
Laboratory:
Centre de Génétique Humaine - CHU Sart-Tilman
RIZIV code:
565471-565482
EQA:
  • 2015 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2016 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
Accreditation (ISO 15189):
2022-02-24 / 2026-02-23
Turnaround time (maximum):
1 month
Document(s):
Created:
29 Aug 2019 - 14:17
Changed:
23 Jan 2023 - 11:34
URL:
https://www.chuliege.be/jcms/c_525434/fr/hemoglobinopathies-de-la-chaine-beta-d…