Publications
- Fluorescent multiplex PCR: Fast method for autosomal dominant spinocerebellar ataxias screening2005 | Second Faculty of Medicine
- Diagnostic possibilities of Prader-Willi and of Angelman syndromes2005 | Second Faculty of Medicine
- Molecular genetic analysis of steroid 21-hydroxylase gene2004 | Second Faculty of Medicine
- Hereditary ataxias in the Czech Republic1998 | Second Faculty of Medicine, Central Library of Charles University
- Genotype/phenotype correlations in neuromuscular disorders1998 | Second Faculty of Medicine
- Introduction of molecular genetic diagnosis in syndromes with a hearing defect1998 | Second Faculty of Medicine
- DNA diagnostics of Friedrich's ataxia1997 | Second Faculty of Medicine
- Clinical genetic and molecular genetic screening of fraXa and fraXe1995 | Second Faculty of Medicine, Central Library of Charles University
- Correlation neurophysiological and molecular genetic findings in SCA patientsPublication without faculty affiliation
- The brain MR imaging in patients with myotonic dystrophy DM 12007 | Second Faculty of Medicine
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