Publications
- Recurrent chromosomal breakpoints in patients with myelodysplastic syndromes and complex karyotype versus fragile sites2012 | First Faculty of Medicine
- Maping of breakpoints in patients with MDS and complex karyotype by microarray methodPublication without faculty affiliation
- Genomic imbalances in 73 patients with MDS and complex karyotypesPublication without faculty affiliation
- Molecular cytogenetic studies of complex karyotypes in myelodysplastic syndromes (MDS): conventional cytogenetics, FISH and multiplex FISH (mFISH/mBAND)Publication without faculty affiliation
- Klinický význam rozsahu del(5q) u nemocných s MDS2021 | First Faculty of Medicine, Central Library of Charles University
- Cryptic aberrations may allow more accurate prognostic classification of patients with myelodysplastic syndromes and clonal evolution2020 | First Faculty of Medicine
- ASXL1 gene alterations in patients with isolated 20q deletion2019 | First Faculty of Medicine
- High frequency of dicentric chromosomes detected by multi-centromeric FISH in patients with acute myeloid leukemia and complex karyotype2018 | First Faculty of Medicine
- Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes2016 | First Faculty of Medicine
- Genetic and epigenetic characterization of low-grade gliomas reveals frequent methylation of the MLH3 gene2015 | First Faculty of Medicine
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