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Cystic Fibrosis / related disorders (50 hot spot mutations)

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Full name:
Cystic Fibrosis / related disorders (50 hot spot mutations)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Post-natal Diagnosis,
Prenatal diagnosis
Specimen:
Dried blood spot card,
Peripheral (whole) blood on EDTA,
Amniotic fluid,
Chorionic villi
Method category:
Targeted variant analysis
Method technique:
PCR based technique
Laboratory:
Centre de Génétique Humaine - CHU Sart-Tilman
RIZIV code:
565353-565364
EQA:
  • 2015 Cystic Fibrosis CF Network (Cystic Fibrosis European Network)
  • 2016 Cystic Fibrosis CF Network (Cystic Fibrosis European Network)
  • 2017 Cystic Fibrosis CF Network (Cystic Fibrosis European Network)
  • 2018 Cystic Fibrosis CF Network (Cystic Fibrosis European Network)
  • 2019 Cystic Fibrosis CF Network (Cystic Fibrosis European Network)
  • 2020 Cystic fibrosis CF Network (Cystic Fibrosis European Network)
  • 2020 CF blood spot GenQA (Genomics Quality Assessment)
  • 2022 Cystic fibrosis CF Network (Cystic Fibrosis European Network)
  • 2023 Cystic fibrosis CF Network (Cystic Fibrosis European Network)
Accreditation (ISO 15189):
2022-08-24 / 2026-02-23
Turnaround time (maximum):
2 weeks
Document(s):
Created:
18 Jul 2019 - 15:04
Changed:
16 Jan 2024 - 13:22
URL:
https://www.chuliege.be/jcms/c_525412/fr/mucoviscidose-et/ou-agenesie-des-canau…