Orphanet: Molecular diagnosis of Nemaline myopathy NEB, Mutation analysis, Carrier screening, PGD
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Molecular diagnosis of Nemaline myopathy (NEB, Mutation analysis, Carrier screening, PGD)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 04/01/2009
  • Hadassah Molecular Genetics Laboratory
  • Hadassah Department of Human Genetics
  • Hadassah Ein Kerem - Hebrew University Medical Center
  • Kiryat Hadassah Ein kerem
  • JERUSALEM 91120
  • ISRAEL
  • Director of laboratory : Dr Israela LERER
  • More information
  • Phone : 972(0)26776931
  • Additional Phone : -
  • Fax : 972(0)26777499
  • Website
  • Contact
Last update: January 2009

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 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.