Publications
- Heterochromatin variants in human karyotypes: a possible association with reproductive failure2014 | First Faculty of Medicine
- 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 variants of chromosome 9: clinical aspects and method of molecular cytogenetic examinationPublication without faculty affiliation
- Heterochromatin area of chromosome 9. Evolution aspects and methods of molecular cytogenetic diagnostics for clinical practicePublication without faculty affiliation
- Alu-mediated Xq24 deletion encompassing CUL4B, LAMP2, ATP1B4, TMEM255A, and ZBTB33 genes causes Danon disease in a female patient2020 | First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine
- Základy biologie a genetiky člověka2020 | First Faculty of Medicine
- CHROMOSOMAL ABERRATIONS IN ETIOLOGY OF EARLY REPRODUCTIVE FAILURE: ANALYSIS OF 233 CASES2019 | First Faculty of Medicine, Third Faculty of Medicine
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