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heterozygot
Publication
Class
Person
Publication
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publication
Familial hypercholesterolemia - a compound heterozygote or homozygote?
2000 |
Publication without faculty affiliation
publication
Increased Risk of Malignancies in Heterozygotes in Families of Patients with Nijmegen Breakage Syndrome
2006 |
Second Faculty of Medicine
publication
Advantage of heterozygotes and evolution of populations
2001 |
Faculty of Science
publication
Tumor supressor gene NBS1 among children patients with malignancies
2004 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Familiar hypercholesterolaemia - combinet hetorozygote or homozygote?
Publication without faculty affiliation
publication
The importance of being heterozygote: Effects of RHD-genotype-sex interaction on the physical and mental health of a non-clinical population
+1
2021 |
Faculty of Science
publication
Clinical significance of heterozygotic mutations of the HFE gene in chronic hepatitis C
2007 |
Third Faculty of Medicine
publication
LAMP2 exon-copy number variations in Danon disease heterozygote female probands: Infrequent or underdetected?
2018 |
Central Library of Charles University, First Faculty of Medicine, Second Faculty of Medicine
publication
The leukemia inhibitory factors gene mutations in the population of infertile women: the heterozygote transition G to A on the position 3400 does not affect the outcome of the infertility treatment.
2007 |
Central Library of Charles University
publication
Heterozygous carriers of Slavic mutation 657del5 of NBN gene in patients with colorectal cancer
2011 |
Second Faculty of Medicine
publication
Cancer risk of heterozygotes with the NBN founder mutation
2007 |
Second Faculty of Medicine
publication
Teratogenic phenylketonuria-related embryopathy
2007 |
Second Faculty of Medicine
publication
Mutations in tumor suppressor gene NBS1 in adult patients with malignancies
2006 |
Second Faculty of Medicine
publication
Heterozygotic form of chronic granulomatous disease
Publication without faculty affiliation
publication
Heterozygotic Form of Chronic Granulomatous Disease
Publication without faculty affiliation
publication
MedPed - the reality of familial hypercholesterolemia care at the biggest center
2018 |
First Faculty of Medicine
publication
Heterozygote Advantage Probably Maintains Rhesus Factor Blood Group Polymorphism: Ecological Regression Study
2016 |
Faculty of Science
publication
Essential defects of athymic nude mice affect also the nu/+ heterozygotes.
1998 |
Faculty of Physical Education and Sport
publication
The cause of hereditary hearing loss in GJB2 heterozygotes-a comprehensive study of the GJB2/DFNB1 region
2021 |
Second Faculty of Medicine
publication
The leukemia inhibitory factors gene mutations in the population of infertile women: the heterozygote transition G to A on the position 3400 does not affect the outcome of the infertility treatment.
2007 |
Central Library of Charles University, Faculty of Medicine in Pilsen
publication
The leukemia inhibitory factors gene mutations in the population of infertile women: the heterozygote transition G to A on the position 3400 does not affect the outcome of the infertility treatment.
2007 |
Faculty of Medicine in Pilsen, First Faculty of Medicine
publication
Immunological findings in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) and their family members: are heterozygotes subclinically affected?
2002 |
Third Faculty of Medicine
publication
Relationship between X-inactivation and clinical involvement in Fabry heterozygotes. Eleven novel mutations in the alpha-galactosidase A gene in the Czech and Slovak population
2005 |
First Faculty of Medicine
publication
Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes
2000 |
Publication without faculty affiliation
publication
Post-mortem Diagnosis of Fabry s Disease in a Female Heterozygote Leading to the Recognition of Undiagnosed Manifest Disease in the Family.
1999 |
Faculty of Physical Education and Sport
publication
A method for detection of germinal mutations in the p53 tumor suppressor gene
1996 |
Second Faculty of Medicine
publication
Mutations in Tumor Suppressor Gene NBS1 in Adult Patients with Malignancies
2006 |
First Faculty of Medicine
publication
The role of balancing selection in maintaining human RhD blood group polymorphism: A preregistered cross-sectional study
2021 |
Faculty of Science
publication
Maternal RhD heterozygous genotype is associated with male biased secondary sex ratio
2020 |
Faculty of Science, First Faculty of Medicine