Orphanet: Diagnostik des HNPCC Syndroms Gene: MLH1, MSH2, MSH6, PMS2
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Diagnosis of HNPCC syndrome (MLH1, MSH2, MSH6, PMS2 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 01/09/2016
  • Phone : 49 (0)234 32 23839
  • Additional Phone : -
  • Fax : 49 (0)234 32 14196
  • Website
Last update: September 2016

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (4)

Quality management

EQA
 EQA

EQA scheme(s) organized by EMQN

HNPCC (Hereditary non-polyposis colon cancer)
2017, 2019
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