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Emberger syndrome / Immunodeficiency 21

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Full name:
Emberger syndrome / Immunodeficiency 21
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Sequence analysis: entire coding region
Deletion/duplication analysis
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centrum Menselijke Erfelijkheid - KUL
RIZIV code:
565471-565482
Turnaround time (maximum):
4-6 months
Document(s):
Created:
19 Jul 2019 - 09:54
Changed:
14 Oct 2021 - 16:03
URL:
https://laboboeken.nexuzhealth.com/pboek/internet/GHB%20CME/14676