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Fragile X syndrome/POF/FXTAS - CGG repeat expansion

Genetic test Export to PDF
Full name:
Fragile X syndrome/POF/FXTAS - CGG repeat expansion
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
Method category:
Targeted variant analysis
Method technique:
PCR based technique
Laboratory:
Centre de Génétique Humaine - Erasme ULB
RIZIV code:
565375-565386
EQA:
  • 2016 Fragile X Syndrome EMQN
  • 2018 Fragile X Syndrome EMQN
  • 2022 Fragile X Syndrome EMQN
Accreditation (ISO 15189):
2021-03-25 / 2024-09-09
Turnaround time (maximum):
2 months
Document(s):
Created:
19 Jul 2019 - 10:55
Changed:
17 Aug 2023 - 13:47
URL:
https://ulbgenetics.be/compendium-des-analyses/#GM90