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Vas deferens, congenital bilateral aplasia of, X-linked (ADGRG2 gene)

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Full name:
Vas deferens, congenital bilateral aplasia of, X-linked (ADGRG2 gene)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Sequence analysis: entire coding region
Mutation screening and sequence analysis of selected exons
Method technique:
Bi-directional Sanger Sequence analysis
Laboratory:
Centrum Medische Genetica - UZ Brussel VUB
RIZIV code:
565471-565482
Accreditation (ISO 15189):
2021-10-07 / 2026-06-14
Turnaround time (maximum):
3 months (10 working days for prenatal diagnosis)
Document(s):
Created:
28 Aug 2019 - 14:33
Changed:
29 Sep 2022 - 10:09