Publications
- Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis2016 | First Faculty of Medicine, Central Library of Charles University
- Klinický význam rozsahu del(5q) u nemocných s MDS2021 | First Faculty of Medicine, Central Library of Charles University
- Concurrent tp53 and cdkn2a gene aberrations in newly diagnosed mantle cell lymphoma correlate with chemoresistance and call for innovative upfront therapy2020 | First Faculty of Medicine, Second Faculty of Medicine
- 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
- Molecular cytogenetic analysis of dicentric chromosomes in acute myeloid leukemia2016 | First Faculty of Medicine
- Change in ploidy status from hyperdiploid to near-tetraploid in multiple myeloma associated with bortezomib/lenalidomide resistance2014 | First Faculty of Medicine
- Clonal evolution in chronic lymphocytic leukemia studied by interphase fluorescence in-situ hybridization2009 | First Faculty of Medicine
- Combined molecular biological and molecular cytogenetic analysis of genomic changes in 146 patients with B-cell chronic lymphocytic leukemia2008 | First Faculty of Medicine
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