- Growth disorders due to rearrangement of SHOX gene locus2019 | Faculty of Medicine in Pilsen
- Léri-Weill Syndrome on the Principle of Structural Aberration of Chromosome Y (Case Report)2018 | Faculty of Medicine in Pilsen
- Complex genetic analysis of SHOX gene in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- Prepubertal Girls With Turner Syndrome and Children With Isolated SHOX Deficiency Have Similar Bone Geometry at the Radius2013 | Faculty of Science, Faculty of Mathematics and Physics, First Faculty of Medicine, Second Faculty of Medicine
- SHOX gene polymorphic variants and their association with isolated short staturePublication without faculty affiliation
- Delece 18p v mozaice u pacienta s fenotypem připomínajícím syndrom Noonanové2016 | Faculty of Mathematics and Physics, First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Bone Geometry and Volumetric Bone Density at the Radius in Patients with Isolated SHOX Deficiency2013 | Faculty of Science, Faculty of Mathematics and Physics, First Faculty of Medicine, Second Faculty of Medicine
- SHOX gene deficiency - a cause of familial short stature2010 | Second Faculty of Medicine
- PAR1 deletion/duplication 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
- Acute lymphoblastic leukemia in a child with Leri-Weill syndrome and complete SHOX gene deletion: A Case Report2018 | Second Faculty of Medicine