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  2. Thalassemia Alpha (2 genes)

Thalassemia Alpha (2 genes)

Genetic test Export to PDF
Full name:
Thalassemia Alpha (2 genes)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
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 - Erasme ULB
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
  • 2020 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2021 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
Accreditation (ISO 15189):
2021-03-25 / 2024-09-09
Turnaround time (maximum):
2 months
Document(s):
Created:
23 Aug 2019 - 08:18
Changed:
19 Jan 2024 - 09:34
URL:
https://ulbgenetics.be/compendium-des-analyses/#GM87