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Human Heredity|January 1, 1992
Complementation in Zellweger syndrome: biochemical analysis of newly generated peroxisomesH Stanczak, K Kremser, A K Singh, et al.Human Heredity|January 1, 1992
Genetic markers in alcoholic liver cirrhosisM V Lareu, A Alvarez-Prechous, C Pardiñas, et al.Human Heredity|January 1, 1992
Distribution of F13A phenotypes in Spain: a particularly high frequency of the F13A*2 alleleJ L Caeiro, E Parra, A Gremo, et al.Human Heredity|March 20, 2004
Robust indices of Hardy-Weinberg disequilibrium for QTL fine mappingHong-Wen Deng, Yu-Mei Li, Miao-Xin Li, et al.Human Heredity|March 20, 2004
A framework for controlling false discovery rates and minimizing the amount of genotyping in the search for disease mutationsEdwin J C G van den Oord, Patrick F SullivanHuman Heredity|September 30, 2005
On confidence intervals for genotype relative risks and attributable risks from case parent trio designs for candidate-gene studiesDaniel Franke, Anne Philippi, Frédéric Tores, et al.Human Heredity|September 3, 2005
Power and sample size calculations for genetic case/control studies using gene-centric SNP maps: application to human chromosomes 6, 21, and 22 in three populationsFrancisco M De La Vega, Derek Gordon, Xiaoping Su, et al.Human Heredity|December 18, 2004
Mapping genes for common diseases: the case for genetic (LD) mapsAndrew Collins, Winston Lau, Francisco M De La VegaHuman Heredity|December 18, 2004
A haplotype-based test of association using data from cohort and nested case-control epidemiologic studiesJinbo Chen, Ulrike Peters, Charles Foster, et al.Human Heredity|April 7, 2005
Comparative informativeness for linkage of multiple SNPs and single microsatellitesEva Lindholm, Susan E Hodge, David A GreenbergPageof 237