- SHOX gene deficiency - a cause of familial short stature2010 | Second Faculty of Medicine
- Analysis of common SHOX gene sequence variants and similar to 4.9-kb PAR1 deletion in ISS patients2014 | First Faculty of Medicine, Faculty of Science
- PAR1 deletion/duplication in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- Complex genetic analysis of SHOX gene in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- SHOX gene deficiency - a cause of familial short stature.2010 | First Faculty of Medicine
