Craniosynostosis / Crouzon syndrome (hot spot mutation - exon 9)
Full name: |
Craniosynostosis / Crouzon syndrome (hot spot mutation - exon 9)
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Test type: |
Clinical
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Test specialty: |
Molecular Genetics
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Test purpose: |
Post-natal Diagnosis,
Prenatal diagnosis
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Specimen: |
Peripheral (whole) blood on EDTA,
Amniotic fluid,
Chorionic villi,
DNA
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Method category: | |
Method technique: | |
Laboratory: | |
RIZIV code: | |
EQA: |
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Turnaround time (maximum): |
21 days
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Document(s): | |
Created: |
20 Aug 2019 - 12:05
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Changed: |
16 Jan 2024 - 13:20
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URL: |