Publications
- Choledochal Cyst with 17q12 Chromosomal Duplication2018 | Second Faculty of Medicine
- MODY in Ukraine: genes, clinical phenotypes and treatment2017 | Second Faculty of Medicine
- Hepatic phenotypes of HNF1B gene mutations: A case of neonatal cholestasis requiring portoenterostomy and literature review2015 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Renal cysts and diabetes syndrome2015 | Second Faculty of Medicine
- Liver, kidneys and diabetes: three faces of HNF1B gene deficit2014 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Lessons from whole-exome sequencing in MODYX families2014 | Second Faculty of Medicine
- MODY diabetes: what should we know for proper diagnostics and treatment?2012 | Second Faculty of Medicine
- Lack of PAX4 mutations in 53 Czech MODYX families2010 | Second Faculty of Medicine
- The genetic landscape of children born small for gestational age with persistent short stature (SGA-SS)2024 | Second Faculty of Medicine
- Integrative role of the SALL4 gene: From thalidomide embryopathy to genetic defects of the upper limb, internal organs, cerebral midline, and pituitary2024 | Second Faculty of Medicine
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