Cystic Fibrosis / Congenital absence of the vas deferens / CFTR-related disorders (88 hot spot mutations)
Full name: |
Cystic Fibrosis / Congenital absence of the vas deferens / CFTR-related disorders (88 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: |
Dried blood spot card,
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): |
2021-03-25 / 2024-09-09
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Turnaround time (maximum): |
3 - weeks
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Document(s): |
Demande-postnat_0723_V9_FR.pdf424.89 KB
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Created: |
18 Jul 2019 - 15:04
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Changed: |
19 Jan 2024 - 09:10
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URL: |