Orphanet: Diagnostic du syndrome X fragile FMR1 gene
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Diagnosis of Fragile X syndrome (FMR1 gene)

  • Laboratoire de Génétique Moléculaire: maladies héréditaires et oncologie
  • Service de biochimie, biologie moléculaire et toxicologie environnementale
  • CHU de Grenoble et des Alpes - Institut de biologie et de pathologie
  • Boulevard de la Chantourne
  • 38043 GRENOBLE CEDEX 9
  • FRANCE
  • Director of laboratory : Dr Julien FAURÉ
  • More information
  • Phone : 33 (0)4 76 76 55 73
  • Additional Phone : -
  • Fax : 33 (0)4 76 76 56 64
  • Website
  • Contact
Last update: February 2020

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
PCR based techniques

List of diseases and genes

List of genes tested (including panels) (1)
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