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Prenatal and postnatal molecular diagnosis of Duchenne and Becker muscular dystrophy, female-carrier testing (deletions and duplications in all exons of DMD gene by MLPA)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 06/08/2013
  • Department of Molecular and Biochemical Genetics
  • Institute of Medical Biology, Genetics and Clinical Genetics, Faculty of Medicine of Comenius University, University Hospital
  • University Hospital Bratislava - Stare mesto
  • Mickiewiczova 13
  • 813 69 BRATISLAVA
  • SLOVAKIA
  • Director of laboratory : Dr Jan CHANDOGA
  • More information
  • Phone : 00421257290192
  • Additional Phone : 00421257290244
  • Fax : -
  • Website
  • Contact
Last update: August 2013

Responsible of diagnostic test

Purpose(s)

Antenatal diagnosis
Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Deletion / Duplication analysis
MLPA based techniques

List of diseases and genes

List of diseases tested (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.