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Noonan syndrome (Screening PTPN11)

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Full name:
Noonan syndrome (Screening PTPN11)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Amniotic fluid,
Chorionic villi
Method category:
Targeted variant analysis
Method technique:
Bi-directional Sanger Sequence analysis
Laboratory:
Centrum Menselijke Erfelijkheid - KUL
RIZIV code:
565456-565460
Accreditation (ISO 15189):
2021-07-08 / 2026-02-02
Turnaround time (maximum):
1o weeks
Document(s):
Created:
22 Jul 2019 - 10:47
Changed:
01 Mar 2023 - 15:58
URL:
https://laboboeken.nexuzhealth.com/pboek/internet/GHB/15589