Orphanet: Diagnostik des nicht polypösen familiären Kolonkarzinoms Gene: MLH1, MSH2, MSH6, PMS2
x

Search for a diagnostic test

* (*) mandatory field

Diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 04/03/2015
  • Zentrum fr Humangenetik Regensburg
  • Universittsklinikum Regensburg
  • Franz-Josef-Strau-Allee 11
  • 93053 REGENSBURG
  • GERMANY
  • Director of laboratory : Pr Ute HEHR
  • More information
  • Phone : 49 (0)941 944 5410
  • Additional Phone : -
  • Fax : 49 (0)941 944 5402
  • Website
  • Contact
Last update: March 2015

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 (2)
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, 2019
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.