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  2. Fragile X syndrome/FXPOI/FXTAS - FMR1 CGG repeat expansion

Fragile X syndrome/FXPOI/FXTAS - FMR1 CGG repeat expansion

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Full name:
Fragile X syndrome/FXPOI/FXTAS - FMR1 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,
Amniotic fluid,
Chorionic villi
Method category:
Targeted variant analysis
Method technique:
PCR based technique
Laboratory:
Centrum Menselijke Erfelijkheid - KUL
RIZIV code:
565375-565386
EQA:
  • 2015 Fragile X Syndrome EMQN
  • 2016 Fragile X Syndrome EMQN
  • 2017 Fragile X Syndrome EMQN
  • 2018 Fragile X Syndrome EMQN
  • 2019 Fragile X Syndrome EMQN
  • 2021 Fragile X Syndrome EMQN
  • 2022 Fragile X Syndrome EMQN
Accreditation (ISO 15189):
2021-07-08 / 2026-02-02
Turnaround time (maximum):
6 - 8 weeks
Document(s):
Created:
19 Jul 2019 - 10:55
Changed:
04 Dec 2023 - 12:27
URL:
https://laboboeken.nexuzhealth.com/pboek/internet/GHB/16838