Orphanet: Diagnosi molecolare della sindrome di Cowden geni PTEN, BMPR1A
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Molecular diagnosis of Cowden syndrome (PTEN, BMPR1A genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 28/07/2009
  • Laboratorio di Genetica Medica
  • Dipartimento di Biomedicina dell'EtÓ Evolutiva
  • Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
  • Piazza Giulio Cesare 11
  • 70124 BARI
  • ITALY
  • Director of laboratory : Pr Nicoletta RESTA
  • More information
  • Phone : 39 080 5593621
  • Additional Phone : -
  • Fax : 39 080 5478269
Last update: July 2009

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (2)
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