Publications
- Mutation analysis of TRPS1 gene including core promoter, 5 ' UTR, and 3 ' UTR regulatory sequences with insight into their organization2017 | Faculty of Science, First Faculty of Medicine, Faculty of Mathematics and Physics
- Comparison of SHOX and associated elements duplications distribution between patients (Lėri-Weill dyschondrosteosis/idiopathic short stature) and population sample2017 | Faculty of Science, First Faculty of Medicine
- Detection of SHOX gene aberrations in routine diagnostic practice and evaluation of phenotype scoring form effectiveness2017 | First Faculty of Medicine
- Analysis of common SHOX gene sequence variants and similar to 4.9-kb PAR1 deletion in ISS patients +12014 | Faculty of Science, First Faculty of Medicine
- SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Léri-Weill dyschondrosteosis2012 | Faculty of Science, First Faculty of Medicine
- SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Leri-Weill dyschondrosteosis2012 | First Faculty of Medicine
- Cryptic chromosomal rearrangements in children with idiopathic mental retardation in the czech population2011 | Faculty of Science, First Faculty of Medicine
- Cryptic Chromosomal Rearrangements in Children with Idiopathic Mental Retardation in the Czech Population2011 | 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
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