Orphanet: Diagnostik des Peutz Jeghers Syndroms STK11 Gen
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Diagnosis of Peutz-Jeghers syndrome (STK11 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 11/05/2009
  • 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: May 2009

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) (1)

Additional information

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.