Cystic Fibrosis / Congenital absence of the vas deferens / CFTR-related disorders (50 hot spot mutations)
Full name: |
Cystic Fibrosis / Congenital absence of the vas deferens / CFTR-related disorders (50 hot spot mutations)
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Test type: |
Clinical
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Test specialty: |
Molecular Genetics
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Test purpose: |
Carrier diagnosis,
Post-natal Diagnosis,
Prenatal diagnosis
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Specimen: |
Peripheral (whole) blood on EDTA,
Chorionic villi,
Amniotic fluid
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Method category: | |
Method technique: | |
Laboratory: | |
RIZIV code: | |
EQA: |
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Accreditation (ISO 15189): |
2023-11-09 / 2024-05-08
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Turnaround time (maximum): |
1 month
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Document(s): | |
Created: |
18 Jul 2019 - 15:04
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Changed: |
22 Jan 2024 - 13:40
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URL: |