Publications
- Patients with Rett syndrome from Czech and Slovak republic: mutation analysis of MECP2 genePublication without faculty affiliation
- Rett syndrome in Czech and Slovak republics: Mutation analysis of MECP2 genePublication without faculty affiliation
- Mutation analysis of MECP2 gene in patients with Rett syndrome from Czech and Slovak RepublicsPublication without faculty affiliation
- Congenital Disorders of Glycosylation Type Ia: Clinical, Biochemical and Molecular Analyses in Two Siblings with Cerebellar Hypoplasia2003 | First Faculty of Medicine
- Clinical and Molecular Analyses in Eight Children with Congenital Disorders of Glycosylation2003 | First Faculty of Medicine
- Molecular Diagnosis of Rett Syndrome: Detection of the Prevalent Mutations in MeCP2 Gene2001 | First Faculty of Medicine
- 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
- Molecular Diagnosis of Rett Syndrome: Detection of the Prevalent Mutations in MeCP2 Gene2001 | Faculty of Physical Education and Sport
- Molecular diagnosis of Rett syndrome: Detection of the prevalent mutation in MeCP2 gene in Czech and Slovak patients2001 | Faculty of Physical Education and Sport
- Congenital erythropoietic porphyria (Gunther disease)2001 | Faculty of Physical Education and Sport
Loading network view...