Orphanet: Molekulare Diagnostik des Noonan ähnlichen Syndroms mit losem Anagenhaar SHOC2 Gen
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Molecular diagnosis of Noonan syndrome-like disorder with loose anagen hair (SHOC2 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 19/01/2018
  • Institut fr Medizinische Genetik
  • Zentrum fr Pathobiochemie und Genetik
  • Medizinische Universitt Wien
  • 1090 WIEN
  • AUSTRIA
  • Director of laboratory : Pr Franco LACCONE
  • More information
  • Phone : +43 (0)1 40160 56531
  • Additional Phone : +43 (0)1 40160 956531
  • Fax : -
  • Website
Last update: January 2018

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 genes tested (including panels) (1)
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