Classes
Publications
- We have a daughter or not? Androgen insensivity syndrome2014 | First Faculty of Medicine
- X-linked Myotubular Myopathy: a Novel Mutation in the MTM-1 Gene - Case Reports2013 | First Faculty of Medicine, Second Faculty of Medicine
- APOE epsilon 4: a potential modulation factor in Rett syndrome2010 | First Faculty of Medicine
- SHOX gene deficiency - a cause of familial short stature.2010 | First Faculty of Medicine
- PAR1 deletion/duplication in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- Complex genetic analysis of SHOX gene in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- SHOX gene polymorphic variants and their association with isolated short staturePublication without faculty affiliation
- Effect of a novel intronic FBN1 mutation on splicing revealed by splicing minigene assayPublication without faculty affiliation
- Použití metody MLPA při diagnostice delecí SHOX genuPublication without faculty affiliation
- ROR2 gene mutation of autosomal recessive Robinow-syndromePublication without faculty affiliation
Loading network view...