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Cystic Fibrosis, newborn screening (12 hot spot mutations; CFTR)

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Full name:
Cystic Fibrosis, newborn screening (12 hot spot mutations; CFTR)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Newborn screening
Specimen:
Dried blood spot card
Method category:
Targeted variant analysis
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centrum Medische Genetica - UZ Antwerpen
RIZIV code:
565353-565364
EQA:
  • 2019 CF blood spot GenQA (Genomics Quality Assessment)
  • 2021 CF blood spot GenQA (Genomics Quality Assessment)
  • 2023 CF blood spot GenQA (Genomics Quality Assessment)
Turnaround time (maximum):
5 days
Document(s):
Created:
29 Nov 2019 - 13:05
Changed:
22 Jan 2024 - 13:41