- Detection of chromosome changes by CGH, array-CGH and SNP array techniques in tumours2014 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Case of 12q24.31 Interstitial Deletion in Association with Intellectual Disability, Dysmorphic Features and Short Stature2013 | Publication without faculty affiliation
- Cytogenetics2013 | Publication without faculty affiliation
- Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing2012 | First Faculty of Medicine
- Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA SequencingPublication without faculty affiliation
- Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing2012 | Second Faculty of Medicine
- Chromophobe renal cell carcinoma - chromosomal aberration variability and its relation to Paner grading system: an array CGH and FISH analysis of 37 cases2013 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Genetická diagnostika epilepsií ve FN Motol aneb význam detekce CNVs pomocí metody array CGH2019 | Second Faculty of Medicine
- An inherited 2q13 deletion in a patient with Marfan syndromePublication without faculty affiliation
- Molecular genetic analysis in 14 Czech Kabuki syndrome patients is confirming the utility of phenotypic scoring2016 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine, Faculty of Medicine in Hradec Králové
- True monozomy of chromosome 5 is presumably not an isolated cytogenetic entity in myelodysplastic syndromes (MDS).Publication without faculty affiliation
- Diagnostic implications of genetic copy number variation in epilepsy plus2019 | Second Faculty of Medicine
- Molecular cloning and analysis of breakpoints on ring chromosome 17 in a patient with autism2008 | Second Faculty of Medicine
- FMR1 Gene Expansion, Large Deletion of Xp, and Skewed X-Inactivation in a Girl With Mental Retardation and Autism2010 | Second Faculty of Medicine
- "Mucin"-secreting papillary renal cell carcinoma: clinicopathological, immunohistochemical, and molecular genetic analysis of seven cases2016 | Faculty of Medicine in Pilsen
- FMR1 Gene Expansion, Large Deletion of Xp, and Skewed X-Inactivation in a Girl With Mental Retardation and Autism2010 | First Faculty of Medicine
- Complex cytogenetic and molecular genetic diagnostics of congenital heart defectsPublication without faculty affiliation
- Utilization of MLPA to detection of genetic changes in neuroblastoma2008 | Second Faculty of Medicine
- Cardiogenetics through cytogenetic eyes - submicroscopic aberration in patients with congenital heart defects2018 | Second Faculty of Medicine
- Delece 18p v mozaice u pacienta s fenotypem připomínajícím syndrom Noonanové2016 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine, Faculty of Mathematics and Physics
- Interstitial del(14)(q) involving IGH: a novel recurrent aberration in B-NHL (1)2007 | First Faculty of Medicine
- Interstitial del(14)(q) involving IGH: a novel recurrent aberration in B-NHL (1)2007 | Faculty of Physical Education and Sport
- Delece 2q13 u pacienta s Marfanovým syndromem2017 | Faculty of Science, First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Uterine smooth muscle tumor analysis by comparative genomic hybridization: a useful diagnostic tool in challenging lesions2015 | First Faculty of Medicine
- Low-grade oncocytic tumour of kidney (CD117-negative, cytokeratin 7-positive): a distinct entity?2019 | Faculty of Medicine in Pilsen
- A girl with an inherited central deletion 22q11.21 resulting in DiGeorge syndrome without typical congenital anomaliesPublication without faculty affiliation
- A girl with an inherited central deletion 22q11.21 resulting in DiGeorge syndrome without typical congenital anomalies2019 | Second Faculty of Medicine, Central Library of Charles University
- The clinical utility of optical genome mapping for the assessment of genomic aberrations in acute lymphoblastic leukemia2021 | Second Faculty of Medicine
- Molecular Cytogenetic Characterization in Four Pediatric Pheochromocytomas and Paragangliomas2011 | Faculty of Science, First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Czech and Slovak Diamond-Blackfan Anemia (DBA) Registry update: Clinical data and novel causative genetic lesions2020 | Central Library of Charles University