- Homeobox gene expression in acute myeloid leukemia is linked to typical underlying molecular aberrations2014 | Second Faculty of Medicine
- Rs868058 in the Homeobox Gene HLX Contributes to Early-Onset Fetal Growth Restriction2022 | Faculty of Medicine in Hradec Králové
- Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects2001 | First Faculty of Medicine
- Fusion of the additional sex combs like 1 and teashirt zinc finger homeobox 2 genes resulting from ider(20q) aberration in a patient with myelodysplastic syndrome2014 | First Faculty of Medicine
- Growth disorders due to rearrangement of SHOX gene locus2019 | Faculty of Medicine in Pilsen
- Low HOX gene expression in PML-RAR-positive leukemia results from suppressed histone demethylation2018 | Second Faculty of Medicine, Central Library of Charles University
- BEL transcription factors in prominent Solanaceae crops: the missing pieces of the jigsaw in plant development2024 | Faculty of Science
- Generation of mRx-Cre Transgenic Mouse Line for Efficient Conditional Gene Deletion in Early Retinal Progenitors2013 | Faculty of Science
- Detection of SHOX gene aberrations in routine diagnostic practice and evaluation of phenotype scoring form effectiveness2017 | 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
- HOX Gene Expression in Phenotypic and Genotypic Subgroups and Low HOXA Gene Expression as an Adverse Prognostic Factor in Pediatric ALL2010 | Faculty of Science, Second Faculty of Medicine
- Role of transcription factors in pituitary embryogenesis2007 | Third Faculty of Medicine
- Role of transcription factors in pituitary embryogenesis2007 | Second Faculty of Medicine
- Genetics of limb defects I: Mirror´s foot - short communication2004 | First Faculty of Medicine
- Genetics of limb defects I: Mirror´s foot - short communication2004 | Faculty of Physical Education and Sport
- Analysis of common SHOX gene sequence variants and similar to 4.9-kb PAR1 deletion in ISS patients2014 | Faculty of Science, First Faculty of Medicine
- Bone Geometry and Volumetric Bone Density at the Radius in Patients with Isolated SHOX Deficiency2013 | Faculty of Science, Second Faculty of Medicine, Faculty of Mathematics and Physics, First Faculty of Medicine
- ASXL1 gene alterations in patients with isolated 20q deletion2019 | First Faculty of Medicine
- Decreased DNA methylation in acute myeloid leukemia patients with DNMT3A mutations and prognostic implications of DNA methylation2012 | First Faculty of Medicine
- 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
- The most valuable predictors of endometrial receptivity2014 | First Faculty of Medicine, Faculty of Physical Education and Sport
- 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
- Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma2019 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Multiple Roles of Pitx2 in Cardiac Development and Disease2017 | First Faculty of Medicine
- Expression of circular RNAs in myelodysplastic neoplasms and their association with mutations in the splicing factor gene SF3B12023 | Faculty of Science, Central Library of Charles University
- Msx1 loss suppresses formation of the ectopic crypts developed in the Apc-deficient small intestinal epithelium2019 | Faculty of Science, Third Faculty of Medicine
- SHOX gene deficiency - a cause of familial short stature2010 | Second Faculty of Medicine
- Neuroblastoma mRNAs Predict Outcome in Children With Stage 4 Neuroblastoma: AEuropean HR-NBL1/SIOPEN Study2014 | Second Faculty of Medicine