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
  • ITALY
  • 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

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) (1)
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.