- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg2005 | First Faculty of Medicine
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg2005 | Faculty of Medicine in Hradec Králové
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321 Arg2005 | Faculty of Medicine in Hradec Králové, Central Library of Charles University
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg2005 | Faculty of Medicine in Hradec Králové, First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321 Arg2005 | Second Faculty of Medicine
- TEL/AML1-Positive Patients Lacking TEL Exon 5 Resemble Canonical TEL/AML1 Cases2011 | Second Faculty of Medicine
- Intrinsically disordered enamel matrix protein ameloblastin forms ribbon-like supramolecular structures via an N-terminal segment encoded by exon 52013 | Faculty of Science
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321 Arg2005 | First Faculty of Medicine
- Laboratory tests of polymorphisms of CYP 2C19-Routine and StatimPublication without faculty affiliation
- A method for detection of germinal mutations in the p53 tumor suppressor gene1996 | Second Faculty of Medicine
- Pregnancy-Associated Plasma Protein A Polymorphisms in Patients with Risk Pregnancies2011 | First Faculty of Medicine
- Fluorescence-based automated fragment analysis of microsatellite polymorphism within the transmembrane region of the MIC-A gene2004 | Third Faculty of Medicine
- Three New PLP1 Splicing Mutations Demonstrate Pathogenic and Phenotypic Diversity of Pelizaeus-Merzbacher Disease2014 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Fluorescence-based automated fragment analysis of microsatellite polymorphism within the transmembrane region of the MIC-A gene2004 | Central Library of Charles University
- Severe atopic dermatitis in a patient with Loeys-Dietz syndrome treated with dupilumab2023 | Third Faculty of Medicine
- TP53 gene mutations are rare in nondysplastic Barrett's esophagus2006 | Second Faculty of Medicine
- FLCN gene-mutated renal cell neoplasms: Mother and daughter cases with a novel germline mutation2012 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Optimization of diagnostic strategy for non-invasive cell-free foetal RHD determination from maternal plasma2021 | First Faculty of Medicine
- An undifferentiated sarcoma with BCOR-CCNB3 fusion transcript - pathological and clinical retrospective study2018 | Second Faculty of Medicine
- Production of recombinant human ameloblastin by a fully native purification pathway2022 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Ornithine carbamoyltransferase deficiency: molecular characterization of 29 families2013 | First Faculty of Medicine
- Characterization of AMBN I and II Isoforms and Study of Their Ca(2+)-Binding Properties2020 | Faculty of Science, First Faculty of Medicine, Central Library of Charles University, Faculty of Physical Education and Sport
- Characterization of AMBN I and II Isoforms and Study of Their Ca2+-Binding Properties2020 | Faculty of Science, First Faculty of Medicine, Central Library of Charles University, Faculty of Physical Education and Sport
- Comprehensive Assessment of BARD1 Messenger Ribonucleic Acid Splicing With Implications for Variant Classification2019 | First Faculty of Medicine
- Non-invasive fetal RHD and RHCE genotyping from maternal plasma in alloimmunized pregnancies2005 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- A novel SMARCA2-CREM fusion expending the molecular spectrum of salivary gland hyalinazing clear cell carcinoma beyond the FET genes2023 | Faculty of Medicine in Pilsen
- A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findings2021 | Faculty of Science
- Expression of four major WT1 splicing variants in acute and chronic myeloid leukemia patients analyzed by newly developed four real-time RT PCRs2012 | Faculty of Science
- Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathy2008 | Publication without faculty affiliation
- Two Li-Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumours1998 | Second Faculty of Medicine