- Advanced childhood MDS: a complex karyotype but not monosomy 7 is an independent prognostic factorPublication without faculty affiliation
- Numerical chromosomal changes (monosomy 7, trisomy 8 and trisomy 21) detected by interphase FISH in children with myeloid disordersPublication without faculty affiliation
- Non-informative results and monosomies in PGD: the importance of a third round of re-hybridization2009 | Central Library of Charles University
- Non-informative results and monosomies in PGD: the importance of a third round of re-hybridization2009 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Refractory anemia in childhood: a retrospective analysis of 67 patients with particular reference to monosomy 72003 | Second Faculty of Medicine
- Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome2024 | Second Faculty of Medicine
- Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 71999 | Second Faculty of Medicine
- True monosomy of chromosome 5 is presumably not an isolated cytogenetic entity in MDSPublication without faculty affiliation
- Non-informative results and monosomies in PGD: the importance of a third round of re-hybridization2009 | Faculty of Medicine in Pilsen
- A complex karyotype but not monosomy 7 is an independent prognostic factor in advanced childhood MDSPublication without faculty affiliation
- Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival2012 | Second Faculty of Medicine
- Numerical chromosomal aberrations (monosomy 7, trisomy 8 and trisomy 21) ascertained by I-FISH in children with myeloid disordersPublication without faculty affiliation
- Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms2022 | First Faculty of Medicine, Second Faculty of Medicine
- Growth disorder in a Vietnamese girl with Turner syndrome and with an uncommon cytogenetic finding2014 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- True monozomy of chromosome 5 is presumably not an isolated cytogenetic entity in myelodysplastic syndromes (MDS).Publication without faculty affiliation
- Genomic imbalances in 73 patients with MDS and complex karyotypesPublication without faculty affiliation
- A novel recurrent chromosomal aberration involving chromosome 7 in childhood myelodysplastic syndrome2010 | First Faculty of Medicine
- Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features2022 | First Faculty of Medicine, Second Faculty of Medicine
- Prognostic Impact of Specific Chromosomal Aberrations in a Large Group of Pediatric Patients With Acute Myeloid Leukemia Treated Uniformly According to Trial AML-BFM 982010 | First Faculty of Medicine
- SNP Array and Phenotype Correlation Shows That FLI1 Deletion Per se is Not Responsible for Thrombocytopenia Development in Jacobsen Syndrome2012 | Publication without faculty affiliation
- Cytogenetics in pediatric MDS - Data of the EWOG-MDS 98 StudyPublication without faculty affiliation
- Incidence, diagnosis and treatment of myelodysplastic syndrome in children in the Czech Republic: results of the prospective study of the EWOG-MDS 1998-20022003 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Cytogenetic abnormalities predict survival after allogeneic hematopoietic stem cell transplantation for pediatric acute myeloid leukemia: a PDWP/EBMT study2024 | Second Faculty of Medicine
- Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents2016 | Second 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
- LIN28B overexpression defines a novel fetal-like subgroup of juvenile myelomonocytic leukemia2016 | Second Faculty of Medicine
- Complex karyotype newly defined: the strongest prognostic factor in advanced childhood myelodysplastic syndrome2010 | Second Faculty of Medicine
- Association of Unbalanced Translocation der(1;7) with Germline GATA2 Mutations2021 | First Faculty of Medicine, Second Faculty of Medicine
- Recurrent deletions of IKZF1 in pediatric acute myeloid leukemia2015 | Second Faculty of Medicine
- A novel recurrent chromosomal aberration involving chromosome 7 in childhood myelodysplastic syndrome2010 | Second Faculty of Medicine