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  2. Beckwith-Wiedemann syndrome (11p15 methylation)

Beckwith-Wiedemann syndrome (11p15 methylation)

Genetic test Export to PDF
Full name:
Beckwith-Wiedemann syndrome (11p15 methylation)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Chorionic villi,
Amniotic fluid
Method category:
Methylation analysis
Method technique:
MLPA based techniques
Laboratory:
Centrum Menselijke Erfelijkheid - KUL
RIZIV code:
565456-565460
EQA:
  • 2016 Beckwith - Wiedermann & Silver-Russell syndromes EMQN
  • 2019 Beckwith - Wiedermann & Silver-Russell syndromes EMQN
  • 2021 Beckwith - Wiedermann & Silver-Russell syndromes EMQN
Accreditation (ISO 15189):
2021-07-08 / 2026-02-02
Turnaround time (maximum):
8- 13 weeks
Document(s):
Created:
18 Jul 2019 - 09:17
Changed:
04 Dec 2023 - 12:53
URL:
https://laboboeken.nexuzhealth.com/pboek/internet/GHB/12268