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Human Genetics|June 23, 2006
Regional distribution of mutations of the ATP7B gene in patients with Wilson disease: impact on genetic testingPeter FerenciHuman Genetics|June 23, 2006
An angiotensin converting enzyme haplotype predicts survival in patients with end stage renal diseaseJames B Wetmore, Kirsten L Johansen, Saunak Sen, et al.Human Genetics|April 29, 2006
A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes I: general principles and overviewJian-Min Chen, Claude Férec, David N CooperHuman Genetics|September 6, 2006
Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populationsT H Beaty, J B Hetmanski, M D Fallin, et al.Human Genetics|September 16, 2006
Identifying genes underlying skin pigmentation differences among human populationsSean Myles, Mehmet Somel, Kun Tang, et al.Human Genetics|October 1, 1990
Chromosomal aberrations in patients with primary biliary cirrhosisA Notghi, U Nestle, G Rittner, et al.Human Genetics|September 29, 2006
Elevated male European and female African contributions to the genomes of African American individualsJoanne M Lind, Holli B Hutcheson-Dilks, Scott M Williams, et al.Human Genetics|June 1, 1990
Fetal hemoglobin in normal adults and beta-thalassemia heterozygotesA Kutlar, F Kutlar, L G Gu, et al.Human Genetics|November 1, 1990
Rare McArdle disease locus polymorphic site on 11q13 contains CpG sequenceR V Lebo, L A Anderson, S DiMauro, et al.Human Genetics|August 1, 1990
Inheritance of some electrophoretic phenotypes of human hairM Schimkat, M P Baur, J HenkePageof 957