Publications
- Absence of spinocerebellar ataxia type 3/Machado-Joseph disease within ataxic patients in the Czech population2005 | Second Faculty of Medicine
- Diagnostic possibilities of Prader-Willi and of Angelman syndromes2005 | Second Faculty of Medicine
- Molecular etiopathogenesis of spinal muscular atrophy2002 | Second Faculty of Medicine
- Radioactive PCR for the screening and diagnostics of fragile X chromosome syndrome - FRAXA2000 | Second Faculty of Medicine, Central Library of Charles University
- DNA diagnosis of the fragile X chromosome syndrome - FRAXA using PCR1998 | Second Faculty of Medicine
- DNA diagnostics of Friedrich's ataxia1997 | Second Faculty of Medicine
- Electrophysiological findings in neuromuscular diseases associated with chromosomal anomaliesPublication without faculty affiliation
- 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
- Fluorescent multiplex PCR: Fast method for autosomal dominant spinocerebellar ataxias screening2005 | Second Faculty of Medicine
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