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Fanconi anemia (FANCC) (hot spot mutation - c.456+4A>T)

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Full name:
Fanconi anemia (FANCC) (hot spot mutation - c.456+4A>T)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Targeted variant analysis
Method technique:
Single nucleotide extension
Laboratory:
Centrum Medische Genetica - UZ Antwerpen
RIZIV code:
565390-565401
Turnaround time (maximum):
1 month
Document(s):
Created:
30 Jul 2019 - 09:58
Changed:
14 Dec 2022 - 11:59
URL:
https://labogidsmedgen.uza.be/analyses/fanconi-anemie-type-c