Orphanet: Diagnosi molecolare dell_acondrogenesi tipo 1B gene SLC26A2

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Molecular diagnosis of achondrogenesis type 1B (SLC26A2 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 02/03/2011
  • UnitÓ di Biochimica
  • Dipartimento di Medicina Molecolare
  • UniversitÓ degli Studi di Pavia - Biochimica '' A. Castellani''
  • Via Taramelli 3/B
  • 27100 PAVIA
  • Director of laboratory : Pr Antonio ROSSI
  • More information
  • Phone : 39 0382 987235
  • Additional Phone : -
  • Fax : 39 0382 423108
  • Website
Last update: March 2011

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics

List of diseases and genes

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