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 11/01/2016
  • Labor Dr. Wisplinghoff
  • laboratoriumsmedizin köln - Dres. med. Wisplinghoff und Kollegen
  • Horbeller Str. 18-20
  • 50858 KÖLN
  • GERMANY
  • Director of laboratory : Dr Uta WISPLINGHOFF
  • More information
  • Phone : 49 (0)221 940 505 0
  • Additional Phone : -
  • Fax : 49 (0)221 940 505 950
  • Website
Last update: January 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)
2015

EQA scheme(s) organized by INSTAND

Molekulargenetik SET 14 (MSH2, MLH1)
2016
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.