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 25/04/2017
  • Institut für Humangenetik
  • Zentrum Pathologie, Forensik und Genetik
  • Medizinische Hochschule Hannover
  • Carl-Neuberg-Str. 1
  • 30625 HANNOVER
  • GERMANY
  • Director of laboratory : Pr Brigitte SCHLEGELBERGER
  • More information
  • Phone : 49 (0)511 532 4520
  • Additional Phone : -
  • Fax : 49 (0)511 532 4521
  • Website
  • Contact
Last update: April 2017

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
Deletion / Duplication analysis
MLPA based techniques

List of diseases and genes

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

Additional information

Quality management

EQA
 EQA

EQA scheme(s) organized by EMQN

HNPCC (Hereditary non-polyposis colon cancer)
2016, 2017, 2018
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