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Molecular diagnosis of 46, XY gonadal dysgenesis (CBX2, DHH, NR5A1, SOX9, and SRY genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 12/01/2018
  • Institut für Medizinische Genetik
  • Zentrum für Pathobiochemie und Genetik
  • Medizinische Universität Wien
  • 1090 WIEN
  • 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


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) (5)
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