Publications
- 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 polymorphic variants and their association with isolated short staturePublication without faculty affiliation
- Gitelman Syndrome as a Cause of Psychomotor Retardation in a Toddler2013 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele2013 | First Faculty of Medicine
- Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families2013 | 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
- TRPC6 gene variants in Czech adult patients with focal segmental glomerulosclerosis and minimal change disease2012 | First Faculty of Medicine
- Gitelman syndrome: novel mutation and long-term follow-up2012 | First Faculty of Medicine
Loading network view...