Orphanet: Molecular diagnosis of laminopathies LMNA related disorders: Hutchinson Gilford Progeria, Atypical Werner syndrome, Mandibuloacral Dysplasia...
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Molecular diagnosis of laminopathies (LMNA-related disorders: Hutchinson-Gilford Progeria, Atypical Werner syndrome, Mandibuloacral Dysplasia...)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 28/06/2012
  • Labor Molekulargenetik
  • Abteilung Medizinische Genetik
  • Universitätsspital Basel
  • Schönbeinstrasse 40
  • 4031 BASEL
  • SWITZERLAND
  • Director of laboratory : Pr Karl HEINIMANN
  • More information
  • Phone : 0041 (0)61 265 36 20
  • Additional Phone : -
  • Fax : 0041 (0)61 265 36 21
  • Website
Last update: June 2012

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)

Additional information

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.