Publications
- 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
- Mantle cell lymphoma-variant Richter syndrome: Detailed molecular-cytogenetic and backtracking analysis reveals slow evolution of a pre-MCL clone in parallel with CLL over several years2016 | First Faculty of Medicine, Second 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
- Primary and recurrent diffuse astrocytomas: genomic profile comparison reveals acquisition of biologically relevant aberrations2016 | First Faculty of Medicine
- Genetic and epigenetic characterization of low-grade gliomas reveals frequent methylation of the MLH3 gene2015 | First Faculty of Medicine
- Acquired uniparental disomy in bone-marrow cells of patients with myelodysplastic syndrome and complex karyotype2015 | First Faculty of Medicine
- An unusual case of high hyperdiploid childhood ALL with cryptic BCR/ABL1 rearrangement2014 | First Faculty of Medicine, Second 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
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