- Late-onset endothelin receptor blockade in hypertensive heterozygous REN-2 transgenic rats2008 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
- Comparison of the characteristics at diagnosis and treatment of children with heterozygous familial hypercholesterolaemia (FH) from eight European countries2020 | First Faculty of Medicine
- ODYSSEY FH I and FH II: 78 week results with alirocumab treatment in 735 patients with heterozygous familial hypercholesterolaemia2015 | First Faculty of Medicine
- Development of Soft Tissue Sarcomas in Ribosomal Proteins L5 and S24 Heterozygous Mice2016 | Central Library of Charles University
- The frequency of venous thromboembolism in women with FV Leiden in heterozygous form from the East Bohemia region in association with pregnancy and puerperiumPublication without faculty affiliation
- Heterozygous carriers of Slavic mutation 657del5 of NBN gene in patients with colorectal cancer2011 | Second Faculty of Medicine
- Does the asymptomatic carriage of FV Leiden and FII prothrombin in heterozygous configuration represent the inccreased risk of thrombembolic complications during pregnancy, childbirth and postpartum?2012 | Publication without faculty affiliation
- Multiple vascular involment in young male with heterozygous familial hypercholesterolemiaPublication without faculty affiliation
- Comparison of the mutation spectrum and association with pre and post treatment lipid measures of children with heterozygous familial hypercholesterolaemia (FH) from eight European countries2021 | First Faculty of Medicine
- Mosaicism for GJB1 mutation causes milder Charcot-Marie-Tooth X1 phenotype in a heterozygous man than in a manifesting heterozygous woman2013 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Science, Faculty of Physical Education and Sport
- Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?2017 | Second Faculty of Medicine
- Hearing Function in Heterozygous Carriers of a Pathogenic GJB2 Gene Mutation2013 | Second Faculty of Medicine
- Rare heterozygous GDF6 variants in patients with renal anomalies2020 | Second Faculty of Medicine
- Prevalence of heterozygous HFE gene mutation in chronic liver disease2007 | First Faculty of Medicine, Third Faculty of Medicine
- Case report: Two heterozygous pathogenic variants of CYP24A1: A novel cause of hypercalcemia and nephrocalcinosis in adulthood2023 | Second Faculty of Medicine, Third Faculty of Medicine
- Heterozygous Nme7 Mutation Affects Glucose Tolerance in Male Rats2021 | First Faculty of Medicine
- A New Concept in Preparation of Reference Materials with Heterozygous Genotype for Molecular Diagnostic Purposes2014 | Faculty of Medicine in Hradec Králové
- Corneal Endothelial Findings in a Czech Patient with Compound Heterozygous Mutations in KERA2014 | First Faculty of Medicine
- NBN 657del5 heterozygous mutations and colorectal cancer risk in the Czech Republic2009 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
- Castration Has Antihypertensive and Organoprotective Effects in Male but Not in Female Heterozygous Ren-2 Rats2011 | Second Faculty of Medicine
- Rh heterozygous mothers have more sons. Trivers-Willard in action?2019 | First Faculty of Medicine, Faculty of Science
- Autoimmune Lymphoproliferative Syndrome with Somatic Fas Mutations2004 | Second Faculty of Medicine
- Congenital polycythemia with homozygous and heterozygous mutations of von Hippel-Lindau gene: five new Caucasian patients2005 | First Faculty of Medicine
- Congenital polycythemia with homozygous and heterozygous mutations of von Hippel-Lindau gene: five new Caucasian patients2005 | Faculty of Physical Education and Sport
- Early-onset endothelin receptor blockade in hypertensive heterozygous Ren-2 rats2006 | Third Faculty of Medicine
- Heterozygous connexin 50 mutation affects metabolic syndrome attributes in spontaneously hypertensive rat2016 | First Faculty of Medicine
- Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function ZEB1 Alleles2021 | First Faculty of Medicine
- Preparing Triple-Compound Heterozygous Control Material for Molecular Diagnostics of TPMT Allelic Variants2015 | Faculty of Medicine in Hradec Králové, Faculty of Pharmacy in Hradec Králové
- Heterozygous gene mutation for ABCG5 transporter in patient with sitosterolemiaPublication without faculty affiliation
- Thyroid hormone resistence due to heterozygous deletion in the gene for T3 receptorPublication without faculty affiliation