Orphanet: Diagnostic du syndrome de Peutz Jeghers Panel
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Diagnosis of Peutz-Jeghers syndrome (Panel)

  • Service de génétique et biologie moléculaires
  • Biologie, Pharmacie, pathologie
  • CHU Paris Centre - Hôpital Cochin, Site Cochin
  • 27 rue du Faubourg Saint-Jacques
  • 75014 PARIS
  • FRANCE
  • Director of laboratory : Pr Michel VIDAUD
  • More information
  • Phone : 33 (0)1 58 41 15 23
  • Additional Phone : -
  • Fax : 33 (0)1 58 41 15 80
  • Website
Last update: February 2020

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
MLPA based techniques
Targeted mutation analysis
NGS sequencing (except WES)
Sequence analysis: entire coding region
NGS sequencing (except WES)
Deletion / Duplication analysis
MLPA based techniques

List of diseases and genes

List of genes tested (including panels) (4)
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