Publications
- Molecular etiopathogenesis of spinal muscular atrophy2002 | Second Faculty of Medicine
- High-resolution melting analysis for detection of MYH9 mutations2008 | Second Faculty of Medicine
- Mutated or non-mutated? Which database to choose when determining the IgVH hypermutation status in chronic lymphocytic leukemia?2006 | 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
- Can ataxin-2 be down-regulated by allele-specific de novo DNA methylation in SCA2 patients?2004 | Second Faculty of Medicine
- Molecular genetic analysis of steroid 21-hydroxylase gene2004 | Second Faculty of Medicine
- Neurogenetics of muscular dystrophies and congenital myopathies2004 | Second Faculty of Medicine
- Detection of deletions and uniparental disomies in Prader-Willi and Angelman syndromes - methodical and interpretational aspects2000 | Second Faculty of Medicine
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