- Gene symbol: MECP2. Disease: Rett syndrome2008 | First Faculty of Medicine
- Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms2007 | Second Faculty of Medicine
- Molecular Diagnosis of Rett Syndrome: Detection of the Prevalent Mutations in MeCP2 Gene2001 | Faculty of Physical Education and Sport
- APOE epsilon 4: a potential modulation factor in Rett syndrome2010 | First Faculty of Medicine
- Molecular diagnosis of Rett syndrome: mutation analysis of the MECP2 genePublication without faculty affiliation
- Mutation analysis of MECP2 gene: Detection of three novel mutations, and two neovel polymorphismsPublication without faculty affiliation
- Rett Syndrome2009 | First Faculty of Medicine
- Patients with Rett syndrome from Czech and Slovak republic: mutation analysis of MECP2 genePublication without faculty affiliation
- 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
- The detection of hot spot mutations in exon three of MECP2 gene in Rett syndrom patients of Slavic originPublication without faculty affiliation
- The detection of hot spot mutations in exon three of MECP2 gene in Rett syndrom patients of Slavic origin2001 | Faculty of Physical Education and Sport
- Mutation analysis of the MECP2 gene in patiens with Rett syndromePublication without faculty affiliation
- Mutation analysis of the MECP2 gene in patients with Rett syndrome +1Publication without faculty affiliation
- Mutational Analysis of the MECP2 Gene in Patients with Rett SyndromePublication without faculty affiliation
- MECP2 mutation detection in Rett patiens from Czech and Slovak RepublicePublication without faculty affiliation
- Mutations in the MECP2 gene in patiens of Slavonic origin with Rett syndromePublication without faculty affiliation
- Rett syndrome in Czech and Slovak republics: Mutation analysis of MECP2 genePublication without faculty affiliation
- Molecular Diagnosis of Rett Syndrome: Detection of the Prevalent Mutations in MeCP2 Gene2001 | First Faculty of Medicine
- MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning2016 | First Faculty of Medicine
- Mutation analysis of MECP2 gene in patients with Rett syndrome from Czech and Slovak RepublicsPublication without faculty affiliation
- Mutation analysis of the MECP2 gene in Czech, Slovak and Ukrainian patients with Rett syndromePublication without faculty affiliation
- A case of Rett syndrome from Ukraine - clinical diagnosis confirmed by mutation analysis of the MECP2 gene2004 | First Faculty of Medicine
- A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3 '-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression1999 | Second Faculty of Medicine
- Molecular diagnosis of Rett syndrome: Detection of the prevalent mutation in MeCP2 gene in Czech and Slovak patientsPublication without faculty affiliation
- Molecular diagnosis of Rett syndrome: Detection of the prevalent mutation in MeCP2 gene in Czech and Slovak patients2001 | Faculty of Physical Education and Sport
- Rett syndrome2013 | First Faculty of Medicine
- Mutation analysis of MeCP2 gene in 36 patients with Rett syndrome of Slavic origin: Detection of two novel mutations and one new polymorphismPublication without faculty affiliation
- Novel CDKL5 Mutations in Czech Patients with Phenotypes of Atypical Rett Syndrome and Early-Onset Epileptic Encephalopathy2016 | First Faculty of Medicine, Central Library of Charles University