Classes
Publications
- APOE epsilon 4: a potential modulation factor in Rett syndrome2010 | First Faculty of Medicine
- Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms2007 | First Faculty of Medicine
- Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms2007 | Faculty of Physical Education and Sport
- MECP2 mutation detection in Rett patiens from Czech and Slovak RepublicePublication without faculty affiliation
- Mutation analysis of the MECP2 gene in patients with Rett syndromePublication without faculty affiliation
- Mutations in the MECP2 gene in patiens of Slavonic origin with Rett syndromePublication without faculty affiliation
- Mutational Analysis of the MECP2 Gene in Patients with Rett SyndromePublication without faculty affiliation
- Pierpont syndrome due to mutation c.1337A > G in TBL1XR1 gene2022 | First Faculty of Medicine
- Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities2021 | First Faculty of Medicine, Second Faculty of Medicine
- Fatal neonatal nephrocutaneous syndrome in 18 Roma children with EGFR deficiency2020 | First Faculty of Medicine
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