Classes
- Molecular CytogeneticsD01000132 | Second Faculty of Medicine
- Examination Methods in Medical CytogeneticsD0600022 | Second Faculty of Medicine
- Genetics and Molecular Biology IID0605044 | Second Faculty of Medicine
- Medical BiologyD0801003 | Second Faculty of Medicine
- BiologyD1301035 | Second Faculty of Medicine
- Basics of Genetics and Prenatal Diagnostics +1D19010005 | Second Faculty of Medicine
- OS - Examination Methods in Medical Genetics +1DV01077 | Second Faculty of Medicine
- OS - Geographical MedicineDV01078 | Second Faculty of Medicine
Publications
- A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 172007 | Second Faculty of Medicine
- Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation2006 | Second Faculty of Medicine
- Early development of immunity in diGeorge syndrome2005 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Diagnostic possibilities of Prader-Willi and of Angelman syndromes2005 | Second Faculty of Medicine
- DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion2003 | Second Faculty of Medicine
- Chromosomal examination in medicine2002 | Second Faculty of Medicine
- Microdeletion 22q11: New FISH Probes Identify Different Deletion Types1999 | Second Faculty of Medicine
- Complex chromosomal rearrangement in the boy from the high-risk pregnancy - case reportPublication 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
- Molecular Cytogenetic Diagnostics of Marker Chromosomes: Analysis in Four Prenatal Cases and Long-Term Clinical Evaluation of Carriers2018 | Second Faculty of Medicine
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