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HomeServicesTest guideAngelman / Prader-Willi Syndrome - uniparental disomy - mechanism identification - whole blood
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Angelman / Prader-Willi Syndrome - uniparental disomy - mechanism identification - whole blood

Other tests

Eurofins Biomnis code

DUPO

Synonyms

  • OMIM code : #105830 / #176270

Pre-analytical

  • 5 mL
  • EDTA whole blood
  • Ambient temperature

Further information

  • 5 ml of whole blood on EDTA from each parent (quotation on request) is required to perform this test
  • According to regulation, each request must ALWAYS be accompanied by a consent form signed by the patient and the prescribing pathologist
  • Enclose the specific B12-INTGB request form: Molecular Genetics

Methodology

Microsatellites. Fluorescent sequence analysis (PCR)

Turn around Time

1 week


Pathologist(s) in charge
Biomnis Lyon
Specialty
Genetics
Contact(s)
Dr Grégory EGEA
Dr Laure RAYMOND
Phone(s)
+334 72 80 25 77
+334 72 80 23 68

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