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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 PolymorphismsAlexandre Bureau, Jordie CroteauHuman 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 NguyenHuman Heredity|December 9, 2025
Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMIDavid CurtisHuman Heredity|January 1, 1986
Human MHC class III genes, Bf and C4. Polymorphism, complotypes and association with MHC class I genes in the Finnish populationJ Partanen, S KoskimiesHuman 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 performanceYue Zhai, Claire Bardel, Maxime Vallée, et al.Human Heredity|May 13, 2024
comorbidPGS: An R Package Assessing Shared Predisposition between Phenotypes Using Polygenic ScoresVincent 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 XinjiangYan Li, Chen Cao, Yanfei Luo, et al.Human Heredity|January 1, 1976
Primary hyperlipoproteinaemia in a Danish familyP Strunge, A F TrostmannPageof 237