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HomeServicesTest guideAngelman / Prader-Willi Syndrome - microdeletion screening - mechanism identification - whole blood - postnatal
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Angelman / Prader-Willi Syndrome - microdeletion screening - mechanism identification - whole blood - postnatal Refered Test

Other tests

Eurofins Biomnis code

FPWA

Synonyms

  • OMIM code : #105830 / #176270

Pre-analytical

  • 5 mL
  • Heparin whole blood
  • Ambient temperature

Further information

  • 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

In Situ hybridisation on metaphases

Turn around Time

6 days


Pathologist(s) in charge
Refered Test
Specialty
Cytogenetics
Contact(s)
Dr Marc NOUCHY
Dr Laure RAYMOND
Dr Nicole COUPRIE
Phone(s)
+334 72 80 23 30
+334 72 80 23 68
+334 72 80 10 04

Caption

Refered TestThe pre-analytical conditions and prices are defined on the basis of the requirements of the performing laboratory.

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