Publications
- Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene - Case Report2016 | Second Faculty of Medicine
- Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation2016 | Second Faculty of Medicine
- Molecular genetic analysis of PKHD1 by next-generation sequencing in Czech families with autosomal recessive polycystic kidney disease2015 | First Faculty of Medicine, Second Faculty of Medicine
- Birt-Hogg-Dubé syndrome2012 | Second Faculty of Medicine
- Hereditary diffuse gastric cancer2012 | Second Faculty of Medicine
- Cowden syndrome2009 | Second Faculty of Medicine
- Cases of LiFraumeni syndrome: diagnostic and preventive possibilities2006 | Second Faculty of Medicine
- Hereditary aetiology of cancer diseases and the importance of genetic counselling and testing in oncology2006 | Second Faculty of Medicine
- Chromosomal Aberration in Inborn Cardiac Defects and their Diagnosis Using the FISH Method1999 | Second Faculty of Medicine
- Inherited ichthyoses: molecular causes of the disease in Czech patients2019 | Publication without faculty affiliation
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