Orphanet: Molecular Diagnosis of Lynch Syndrome Comprehensive NGS Panel 4 genes and deldup 4 genes plus EPCAM
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Molecular Diagnosis of Lynch Syndrome- Comprehensive NGS Panel (4 genes) and del/dup (4 genes plus EPCAM)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 22/06/2016
  • Genome Diagnostics and Cancer Cytogenetics
  • University Health Network/Department of Clinical Laboratory Genetics
  • Toronto General Hospital
  • 200 Elizabeth Street
  • M5G 2C4 TORONTO
  • CANADA
  • Director of laboratory : Dr Suzanne KAMEL-REID
  • More information
  • Phone : 01(416)340-4800 x5739/7624
  • Additional Phone : -
  • Fax : 01(416)340-3596
  • Contact
Last update: June 2016

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

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

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (5)
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.