- PAR1 deletion/duplication in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- X:Y translocation associated with dyschondrosteosisPublication without faculty affiliation
- Complex genetic analysis of SHOX gene in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- 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
- 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
- SHOX gene deficiency - a cause of familial short stature.2010 | First Faculty of Medicine
- Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis2016 | First Faculty of Medicine, Central Library of Charles University
- SHOX gene polymorphic variants and their association with isolated short staturePublication without faculty affiliation
- Detection of SHOX gene aberrations in routine diagnostic practice and evaluation of phenotype scoring form effectiveness2017 | First Faculty of Medicine
- Prepubertal Girls With Turner Syndrome and Children With Isolated SHOX Deficiency Have Similar Bone Geometry at the Radius2013 | Faculty of Science, First Faculty of Medicine, Faculty of Mathematics and Physics, Second Faculty of Medicine
- Analysis of common SHOX gene sequence variants and similar to 4.9-kb PAR1 deletion in ISS patients2014 | Faculty of Science, First Faculty of Medicine
- SHOX gene deficiency - a cause of familial short stature2010 | Second Faculty of Medicine