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Cystic Fibrosis / Congenital absence of the vas deferens / related disorders (50 hot spot mutations)

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Full name:
Cystic Fibrosis / Congenital absence of the vas deferens / related disorders (50 hot spot mutations)
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:
565353-565364
EQA:
  • 2017 Cystic Fibrosis CF Network (Cystic Fibrosis European Network)
  • 2020 Cystic fibrosis CF Network (Cystic Fibrosis European Network)
Accreditation (ISO 15189):
2021-07-08 / 2026-02-02
Turnaround time (maximum):
2-4 week
Document(s):
Created:
18 Jul 2019 - 15:04
Changed:
01 Mar 2023 - 14:56
URL:
https://laboboeken.nexuzhealth.com/pboek/internet/GHB%20CME/13903