Publications
- Introduction of molecular genetic diagnosis in syndromes with a hearing defect1998 | Second Faculty of Medicine
- The brain MR imaging in patients with myotonic dystrophy DM 12007 | Second Faculty of Medicine
- Genotype/phenotype correlation in a SCA1 family: anticipation without CAG expansion2005 | Second Faculty of Medicine
- Absence of spinocerebellar ataxia type 3/Machado-Joseph disease within ataxic patients in the Czech population2005 | Second Faculty of Medicine
- 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
- Genetic Polymorphisms of UGT 1A1*28 in the TATA-box Promoter Region of Bilirubin Uridinediphosphate-glucuronosyltransferase Gene in Children with Gilbert's Syndrome2005 | Second Faculty of Medicine
- Electrophysiological findings in patients with ataxia2004 | Second Faculty of Medicine
- Molecular genetic analysis of steroid 21-hydroxylase gene2004 | Second Faculty of Medicine
- Congenital myotonic dystrophy2003 | Second Faculty of Medicine, Central Library of Charles University
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