Orphanet: Molecular diagnosis of Spino Cerebellar Ataxia SCA1, SCA2, SCA3, SCA6, SCA7 , Mutation analysis, PGD
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Molecular diagnosis of Spino Cerebellar Ataxia (SCA1, SCA2, SCA3, SCA6, SCA7 , Mutation analysis, PGD)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 21/06/2009
  • 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: June 2009

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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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.