Orphanet: Diagnostic des syndromes dysmorphologiques par CGH array
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Diagnosis of dysmorphological syndromes by CGH array

Despite our efforts to ensure that data is up to date, this activity has not been validated since 09/08/2012
  • Laboratoire de génétique moléculaire et d'histocompatibilité
  • Pôle de Biologie-Pathologie
  • CHU de Brest - Hôpital de la Cavale Blanche
  • 2 avenue Foch
  • 29609 BREST CEDEX
  • FRANCE
  • Director of laboratory : Pr Claude FEREC
  • More information
  • Phone : 33 (0)2 29 02 01 50
  • Additional Phone : -
  • Fax : 33 (0)2 29 02 01 51
  • Website
  • Contact
Last update: August 2012

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Cytogenetics
Detection of microdeletions/microduplications
Array based techniques

List of diseases and genes

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.