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
- 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
- Molecular cytogenetic analysis of dicentric chromosomes in acute myeloid leukemia2016 | First Faculty of Medicine
- Acquired uniparental disomy in bone-marrow cells of patients with myelodysplastic syndrome and complex karyotype2015 | First Faculty of Medicine
- Involvement of deleted chromosome 5 in complex chromosomal aberrations in newly diagnosed myelodysplastic syndromes (MDS) is correlated with extremely adverse prognosis2014 | First Faculty of Medicine
- Fusion of the additional sex combs like 1 and teashirt zinc finger homeobox 2 genes resulting from ider(20q) aberration in a patient with myelodysplastic syndrome2014 | First Faculty of Medicine
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