Orphanet: Diagnostic du syndrome de Lynch Panel
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Diagnosis of Lynch syndrome (Panel)

  • Laboratoire Mixte de Génétique Constitutionnelle des Cancers Fréquents CLB-HCL
  • CLCC Léon Bérard
  • 28 Rue Laënnec
  • 69373 LYON CEDEX 8
  • FRANCE
  • Director of laboratory : Dr Hong WANG
  • More information
  • Phone : 33 (0)4 78 78 27 23
  • Additional Phone : -
  • Fax : 33 (0)4 78 78 28 68
  • Website
Last update: February 2020

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
Sanger sequencing
Targeted mutation analysis
MLPA based techniques
Mutation scanning/screening and sequence analysis of selected exons
Sanger sequencing
Mutation scanning/screening and sequence analysis of selected exons
NGS sequencing (except WES)
Mutation scanning/screening and sequence analysis of selected exons
PCR based techniques
Sequence analysis: entire coding region
Sanger sequencing
Sequence analysis: entire coding region
NGS sequencing (except WES)
Deletion / Duplication analysis
MLPA based techniques
Deletion / Duplication analysis
NGS sequencing (except WES)
Deletion / Duplication analysis
PCR based techniques

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (7)
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