- Genetic heterogeneity of neuronal intranuclear inclusion disease: What about the infantile variant?2021 | First Faculty of Medicine
- Genetic heterogeneity in infantile spasms2019 | Second Faculty of Medicine
- Stickler syndrome in the Czech Republic: phenotypic variability and genetic heterogeneity2021 | Second Faculty of Medicine
- Genetic heterogeneity of megacystis-microcolon-intestinal hypoperistalsis syndromePublication without faculty affiliation
- Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome2006 | First Faculty of Medicine
- Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in Gypsies2008 | Second Faculty of Medicine
- Identification, by homozygosity mapping, of a novel locus for autosomal recessive congenital ichthyosis on chromosome 17p, and evidence for further genetic heterogeneity2001 | Central Library of Charles University
- Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia2011 | First Faculty of Medicine
- Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia2011 | Second Faculty of Medicine
- Familial juvenile hyperuricemic nephropathy (FJHN): Localization of the gene on chromosome 16P11. 2 and evidence for genetic heterogenityPublication without faculty affiliation
- DNA cloning demonstrates high genetic heterogeneity in populations of the subaerial green alga Trentepohlia (Trentepohliales, Chlorophyta)2019 | Faculty of Science
- Familial juvenile hyperuricemic nephropathy (FJHN): Localization of the gene on chromosome 16P11. 2 and evidence fo genetic heterogeneity (1)Publication without faculty affiliation
- Familial juvenile hyperuricemic nephropathy (FJHN): Localization of the gene on chromosome 16p11. 2-and evidence for genetic heterogenity (3)2000 | First Faculty of Medicine
- Long-term provisional rehabilitation of amelogenesis imperfecta.Publication without faculty affiliation
- Molecular diversity of combined and complex dystonia: insights from diagnostic exome sequencing2017 | First Faculty of Medicine
- HLA in Czech adult patients with autoimmune diabetes mellitus: comparsion with Czech children with type 1 diabetes and patients type 2 diabetes2003 | Third Faculty of Medicine
- Genetics of neurodevelopmental disorders2021 | Second Faculty of Medicine
- Carney complex2011 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Genetic principle of Alzheimer's disease and possibility of its prediction2008 | Publication without faculty affiliation
- Surgical Treatment of Congenital Cleft Foot - Case Study and Literature Review2020 | Faculty of Medicine in Hradec Králové
- Successful use of pulsatile gonadotropin-releasing hormone (GnRH) pregnancy in a patient with GnRH receptor mutations2000 | Faculty of Medicine in Pilsen
- Segregation of a novel p.(Ser270Tyr) MAF mutation and p.(Tyr56*) CRYGD variant in a family with dominantly inherited congenital cataracts2017 | First Faculty of Medicine
- Pheochromocytoma2013 | First Faculty of Medicine
- Introduction of molecular genetic diagnosis in syndromes with a hearing defect1998 | Second Faculty of Medicine
- Clinical and biochemical characterization of syndromes associated with defects of the insulin receptor1992 | Second Faculty of Medicine
- Novel variants in EDNRB gene in Waardenburg syndrome type II and SOX10 gene in PCWH syndrome2021 | Faculty of Medicine in Hradec Králové
- Next generation sequencing and its application in the diagnostics of neuromuscular diseases2021 | Second Faculty of Medicine
- Strategy of treatment of metastatic non-small-cell lung cancer - squamous cell carcinoma2016 | First Faculty of Medicine
- Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB92012 | First Faculty of Medicine
- A novel missense mutation in LIM2 causing isolated autosomal dominant congenital cataract2020 | First Faculty of Medicine