Publications
- Variants of human chromosomes and their significance from the point of view of clinical genetics2012 | First Faculty of Medicine, Third Faculty of Medicine
- Cytogenetic variants in clinical paeditrics practice2012 | First Faculty of Medicine
- Variants of chromosome 9 in the newborn population and their clinical significance2012 | First Faculty of Medicine
- Advanced maternal age as a sole indication for amniocentesis – analysis of 418 fetal karyotypes2011 | First Faculty of Medicine
- SHOX gene polymorphic variants and their association with isolated short staturePublication without faculty affiliation
- Increased risk of reproduction failure in heterochromatine variants carriers?Publication without faculty affiliation
- Cytogenetic variants of chromosoem 9 - incidence, clinical significance and possibilites of molecular-cytogenetic analysis.Publication without faculty affiliation
- Incidence and clinical significance of chromosomal abnormalities of heterochromatin area of human chromosome 9Publication without faculty affiliation
- Heterochromatin variants of human chromosome 9 and the reproduction failurePublication without faculty affiliation
- Heterochromatin area of chromosome 9. Evolution aspects and methods of molecular cytogenetic diagnostics for clinical practicePublication without faculty affiliation
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