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
- 45,X/46,X,psu dic(Y) Gonadal Dysgenesis: Influence of the Two Cell Lines on the Clinical Phenotype, Including Gonadal Histology2013 | Second Faculty of Medicine
- A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 172007 | Second Faculty of Medicine
- Diagnostic possibilities of Prader-Willi and of Angelman syndromes2005 | Second Faculty of Medicine
- Case report of patients with a marker chromosome2004 | Second Faculty of Medicine
- Relationship between Genotype and Phenotype in Patients with Microdeletion of Chromosome 22q112001 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Williams-Beuren syndrome2000 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Chromosomal Aberration in Inborn Cardiac Defects and their Diagnosis Using the FISH Method1999 | Second Faculty of Medicine
- Centromere-specific multicolour FISH - method for the identification of marker-chromosomes : case report demonstrating our first experiencesPublication without faculty affiliation
- 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
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