Publications
- Application of the new insertion-deletion polymorphism kit for forensic identification and parentage testing on the Czech population2013 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families2013 | First Faculty of Medicine
- Broad genetic issues in lung cancer2009 | First Faculty of Medicine
- Molecular genetic investigation of polymorfisms and STR loci in patients with nonsmall cell lung cancer2009 | First Faculty of Medicine
- Huntington's Disease: Experience with Genetic Testing within 1994-20052007 | First Faculty of Medicine
- Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects2007 | First Faculty of Medicine
- The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington´s disease2006 | First Faculty of Medicine
- PAR1 deletion/duplication in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- Complex genetic analysis of SHOX gene in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- MLPA analysis in children with mental retardationPublication without faculty affiliation
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