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Human Heredity|January 1, 1985
A possible clinical implication of homozygous inversions of 9qh regions with Cornelia de Lange syndrome (CLS)K A Babu, R S Verma, J Rodriguez, et al.Human Heredity|January 1, 1986
Frequencies of the GPXT1 (or GPX*2(1) and CA2II alleles in some Congo populationsG Destro-Bisol, A Briziobello, A Adriani, et al.Human Heredity|February 14, 2021
Challenges of Adjusting Single-Nucleotide Polymorphism Effect Sizes for Linkage DisequilibriumValentina Escott-Price, Karl Michael SchmidtHuman Heredity|February 10, 2021
Identification of Influential Variants in Significant Aggregate Rare Variant TestsRachel Z Blumhagen, David A Schwartz, Carl D Langefeld, et al.Human Heredity|February 20, 2017
Human Birth Weight and Reproductive Immunology: Testing for Interactions between Maternal and Offspring KIR and HLA-C GenesMichelle M Clark, Olympe Chazara, Eric M Sobel, et al.Human Heredity|February 8, 2017
How Can We Explain Very Low Odds Ratios in GWAS? I. Polygenic ModelsSusan E Hodge, David A GreenbergHuman Heredity|January 1, 1988
Use of a simple method for the Epstein-Barr virus transformation of lymphocytes from members of large families of Réunion IslandM Ventura, A Gibaud, J Le Pendu, et al.Human Heredity|March 20, 2017
An Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of InheritanceDerek Gordon, Douglas Londono, Payal Patel, et al.Human Heredity|June 9, 1998
Genetic relationships among Japanese, northern Han, Hui, Uygur, Kazakh, Greek, Saudi Arabian, and Italian populations based on allelic frequencies at four VNTR (D1S80, D4S43, COL2A1, D17S5) and one STR (ACTBP2) lociY Katsuyama, H Inoko, T Imanishi, et al.Human Heredity|June 9, 1998
Mapping genes through the use of linkage disequilibrium generated by genetic drift: 'drift mapping' in small populations with no demographic expansionJ D Terwilliger, S Zöllner, M Laan, et al.Pageof 237