- Case Reports of Patients with a Marker Chromosome2004 | Publication without faculty affiliation
- Case report of patients with a marker chromosome2004 | Second Faculty of Medicine
- Two supernumerary marker-chromosomes in a healthy woman: a case reportPublication without faculty affiliation
- Two supernumerary marker-chromosomes in a healthy woman - a case reportPublication without faculty affiliation
- Centromere-specific multicolour FISH - method for the identification of marker-chromosomes : case report demonstrating our first experiencesPublication without faculty affiliation
- Molecular Cytogenetic Diagnostics of Marker Chromosomes: Analysis in Four Prenatal Cases and Long-Term Clinical Evaluation of Carriers2018 | Second Faculty of Medicine
- Case reports of patients with a marker chromosome2004 | Publication without faculty affiliation
- A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy - case report and review of the literature2018 | Second Faculty of Medicine
- 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
- A Multilocus Technique for Risk Evaluation of Patients with Neuroblastoma2011 | Publication 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
- Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes?1992 | Second Faculty of Medicine
- Hypothesis - 45,X Turner Syndrome Does not Exist - All Surviving Patients Have Sex-Chromosomal Mosaicism1991 | Second Faculty of Medicine
- A novel recurrent chromosomal aberration involving chromosome 7 in childhood myelodysplastic syndrome2010 | First Faculty of Medicine
- A novel recurrent chromosomal aberration involving chromosome 7 in childhood myelodysplastic syndrome2010 | Second Faculty of Medicine