Publikace
- Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes2017 | 2. lékařská fakulta
- Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations2016 | 2. lékařská fakulta
- Ancestral mutations may cause a significant proportion of GCK-MODY2012 | 2. lékařská fakulta
- Two Independent Genetic Factors Responsible for the Associations of the IBD5 Locus with Crohn's Disease in the Czech Population2011 | 2. lékařská fakulta
- The CTLA4 variants may interact with the IL23R-and NOD2-conferred risk in development of Crohn's disease2010 | 2. lékařská fakulta
- The genetic landscape of children born small for gestational age with persistent short stature (SGA-SS)2024 | 2. lékařská fakulta
- Integrative role of the SALL4 gene: From thalidomide embryopathy to genetic defects of the upper limb, internal organs, cerebral midline, and pituitary2024 | 2. lékařská fakulta
- SALL4 phenotype in four generations of one family: An interplay of the upper limb, kidneys, and the pituitary2024 | 2. lékařská fakulta
- Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq2024 | 2. lékařská fakulta
- Genetic testing of children with familial tall stature: is it worth doing?2024 | 2. lékařská fakulta
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