Publications
- 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
- Detection of Deletions and Uniparental Disomies in prade-Willi and Angelman Syndromes - Methodical and Interpretational Aspects2000 | Second Faculty of Medicine, Central Library of Charles University
- Radioactive PCR for the screening and diagnostics of fragile X chromosome syndrome - FRAXA2000 | Second Faculty of Medicine, Central Library of Charles University
- Detection of deletions and uniparental disomies in Prader-Willi and Angelman syndromes - methodical and interpretational aspects2000 | Second Faculty of Medicine
- Mutation Analysis of COL4A5 and COL4A3 Genes in Alport´s Syndrome1999 | Second Faculty of Medicine, Central Library of Charles University
- DNA diagnosis of the fragile X chromosome syndrome - FRAXA using PCR1998 | Second Faculty of Medicine
- 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
- The brain MR imaging in patients with myotonic dystrophy DM 12007 | Second Faculty of Medicine
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