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Human Heredity|January 1, 1986
G1m(1) and G1m(2) allotypes in Albanian towns of CalabriaG De Benedictis, G Rose, C Brancati, et al.Human Heredity|January 1, 1988
Human enzyme polymorphism in the Canary Islands. II. African influenceJ M Morilla, J M Afonso, M Hernández, et al.Human Heredity|January 18, 2014
A network-based kernel machine test for the identification of risk pathways in genome-wide association studiesSaskia Freytag, Juliane Manitz, Martin Schlather, et al.Human Heredity|July 31, 2025
Molecular Characterization of Two Hypertension Pedigrees Carrying Mitochondrial tRNAGln 4386T>C MutationZhongshun Luo, Jiayu Lin, Jiazhen Ji, et al.Human Heredity|January 1, 1986
Genetic variants of factor B in a population of JordanH Saleh, C Davrinche, R Charlionet, et al.Human Heredity|October 19, 2020
Novel IDS Variants Identified in Three Unrelated Pakistani Patients Affected with Mucopolysaccharidosis Type II (Hunter Syndrome)Bibi Zubaida, Hajira Batool, Huma Arshad Cheema, et al.Human Heredity|January 1, 1986
Polymorphism of the seventh complement component, C7, in ChineseL J York, W H Marshall, S N HuangHuman Heredity|May 26, 2021
Voltage-Gated Sodium Channel β1 Gene: An OverviewHisham Al-Ward, Chun-Yang Liu, Ning Liu, et al.Human Heredity|December 6, 2019
The Association of Partial Azoospermia Factor C Deletions and Male Infertility in Northwestern ChinaChunlian Liu, Xinyan Zhao, Chunlan Mu, et al.Human Heredity|January 16, 2023
A Comprehensive Study of Disease-Causing Variants in PAH, QDPR, PTS, and PCD Genes in Iranian Patients with Hyperphenylalaninemia: A Systematic ReviewMahmoud Ghanei, Seyedeh Helia Sadat Fatemi, Tayebeh HamzehloueiPageof 237