Craniosynostosis syndromes (Apert, Crouzon)
Full name: |
Craniosynostosis syndromes (Apert, Crouzon)
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Test type: |
Clinical
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Test specialty: |
Molecular Genetics
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Test purpose: |
Post-natal Diagnosis
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Specimen: |
Peripheral (whole) blood on EDTA
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Method category: | |
Method technique: | |
Laboratory: | |
RIZIV code: | |
Turnaround time (maximum): |
2 months
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Document(s): | |
Created: |
20 Aug 2019 - 12:05
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Changed: |
21 Jun 2022 - 12:25
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URL: |