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Molecular diagnosis of Langer Mesomelic Dysplasia and Leri Weill Dyschondrosteosis (SHOX gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 03/08/2009
  • Laboratorium voor Diagnostische Genoomanalyse
  • Afdeling Klinische Genetica
  • LUMC - Leids Universitair Medisch Centrum
  • Albinusdreef 2
  • 2333 ZA LEIDEN
  • NETHERLANDS
  • Director of laboratory : Pr F. [Frank] BAAS
  • More information
  • Phone : 31 (0)71 526 9800
  • Additional Phone : 31 (0)71 526 9810
  • Fax : 31 (0)71 526 8276
  • Website
  • Contact
Last update: August 2009

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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List of diseases and genes

List of genes tested (including panels) (1)

Quality management

EQA
 EQA

EQA scheme(s) organized by EMQN

SHOX (Short stature homeobox gene testing)
2014, 2016
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.