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Human Heredity|April 5, 2001
Offspring risk and sibling risk for multilocus traitsM Koivisto, H MannilaHuman Heredity|November 30, 2000
Epidemiology and factor analysis of obesity, type II diabetes, hypertension, and dyslipidemia (syndrome X) on the Island of Kosrae, Federated States of MicronesiaD Shmulewitz, S B Auerbach, T Lehner, et al.Human Heredity|November 30, 2000
C677T methylenetetrahydrofolate reductase polymorphism is not a risk factor for pre-eclampsia/eclampsia among Australian womenT Kaiser, S P Brennecke, E K MosesHuman Heredity|November 30, 2000
Ascertainment and anticipation in family studiesJ Hoh, D F Heitjan, C Mérette, et al.Human Heredity|November 30, 2000
Association tests for traits with variable age at onsetO Mokliatchouk, D Blacker, D RabinowitzHuman Heredity|November 30, 2000
Identification of mtDNA mutation in a pedigree with gestational diabetes, deafness, Wolff-Parkinson-White syndrome and placenta accretaP Aggarwal, R Gill-Randall, T Wheatley, et al.Human Heredity|January 1, 1975
Information processing in immunogenetic analysis. V. Some irregularities caused by simple-complex transformation of T universesJ HirschfeldHuman Heredity|May 9, 2000
Allele-specific variation in the gene copy number of human cytosine 5-methyltransferaseM Franchina, P H KayHuman Heredity|April 27, 2000
K5 D328E: a novel missense mutation in the linker 12 domain of keratin 5 associated with epidermolysis bullosa simplex (Weber-Cockayne)M Liovic, B Podrumac, V Dragos, et al.Human Heredity|April 27, 2000
Molecular heterogeneity of the glucose-6-phosphate dehydrogenase deficiency in the Hellenic populationP Menounos, C Zervas, G Garinis, et al.Pageof 237