Orphanet: Diagnostik des HNPCC Syndroms Gene: MLH1, PMS2, MSH2, MSH6 und Mikrosatellitendiagnostik
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Diagnosis of HNPCC syndrome (MLH1, PMS2, MSH2, MSH6 genes and microsatellite analysis)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 18/06/2009
  • Abteilung Chirurgische Forschung
  • Universitätsklinikum Carl Gustav Carus an der TU Dresden
  • Fetscherstrasse 74
  • 01307 DRESDEN
  • GERMANY
  • Director of laboratory : Pr Hans K. SCHACKERT
  • More information
  • Phone : 49 (0)351 458 3598
  • Additional Phone : -
  • Fax : 49 (0)351 458 4350
  • Website
  • Contact
Last update: June 2009

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
Biochemical genetics
Protein expression
Immunohistochemistry

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)
2017, 2018
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.