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Human Heredity
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August 1, 2016
When Is an Endophenotype Useful to Detect Association to a Disease? Exploring the Relationships between Disease Status, Endophenotype and Genetic Polymorphisms
Alexandre Bureau, Jordie Croteau
Human Heredity
|
August 3, 2022
The prevalence of JAK2 exon12 mutations in Vietnamese patients with JAK2 V617F-negative polycythemia vera: frequent or rare?
Ngoc T Nguyen, Linh T Nguyen, Xuan T Nguyen
Human Heredity
|
January 1, 1988
Haptoglobin groups in ovarian carcinoma
N Fröhlander, U Stendahl
Human Heredity
|
December 9, 2025
Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI
David Curtis
Human Heredity
|
January 1, 1986
Human MHC class III genes, Bf and C4. Polymorphism, complotypes and association with MHC class I genes in the Finnish population
J Partanen, S Koskimies
Human Heredity
|
January 1, 1986
Distribution of C3 and Bf allotypes in Tuscany (Italy)
R Domenici, A Giari, M Bargagna, et al.
Human Heredity
|
March 17, 2024
Place of concordance-discordance model in evaluating NGS performance
Yue Zhai, Claire Bardel, Maxime Vallée, et al.
Human Heredity
|
May 13, 2024
comorbidPGS: An R Package Assessing Shared Predisposition between Phenotypes Using Polygenic Scores
Vincent Pascat, Liudmila Zudina, Anna Ulrich, et al.
Human Heredity
|
May 20, 2026
Comparative profiles of pediatric Mendeliome: A Single-Centre 572-Whole-Exome Sequencing Study in Xinjiang
Yan Li, Chen Cao, Yanfei Luo, et al.
Human Heredity
|
January 1, 1976
Primary hyperlipoproteinaemia in a Danish family
P Strunge, A F Trostmann
Page
of 237
Search research articles
Search
Showing results (551-560 of 2,367) with videos related to
Sort By:
Page
of 237
Human Heredity
|
August 1, 2016
When Is an Endophenotype Useful to Detect Association to a Disease? Exploring the Relationships between Disease Status, Endophenotype and Genetic Polymorphisms
Alexandre Bureau, Jordie Croteau
Human Heredity
|
August 3, 2022
The prevalence of JAK2 exon12 mutations in Vietnamese patients with JAK2 V617F-negative polycythemia vera: frequent or rare?
Ngoc T Nguyen, Linh T Nguyen, Xuan T Nguyen
Human Heredity
|
January 1, 1988
Haptoglobin groups in ovarian carcinoma
N Fröhlander, U Stendahl
Human Heredity
|
December 9, 2025
Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI
David Curtis
Human Heredity
|
January 1, 1986
Human MHC class III genes, Bf and C4. Polymorphism, complotypes and association with MHC class I genes in the Finnish population
J Partanen, S Koskimies
Human Heredity
|
January 1, 1986
Distribution of C3 and Bf allotypes in Tuscany (Italy)
R Domenici, A Giari, M Bargagna, et al.
Human Heredity
|
March 17, 2024
Place of concordance-discordance model in evaluating NGS performance
Yue Zhai, Claire Bardel, Maxime Vallée, et al.
Human Heredity
|
May 13, 2024
comorbidPGS: An R Package Assessing Shared Predisposition between Phenotypes Using Polygenic Scores
Vincent Pascat, Liudmila Zudina, Anna Ulrich, et al.
Human Heredity
|
May 20, 2026
Comparative profiles of pediatric Mendeliome: A Single-Centre 572-Whole-Exome Sequencing Study in Xinjiang
Yan Li, Chen Cao, Yanfei Luo, et al.
Human Heredity
|
January 1, 1976
Primary hyperlipoproteinaemia in a Danish family
P Strunge, A F Trostmann
Page
of 237