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Human Heredity|January 1, 1996
Asian hypersusceptibility to motion sicknessR M Stern, S Hu, S H Uijtdehaage, et al.Human Heredity|January 1, 1988
Salivary enzyme polymorphisms (Set, Sgd and AMY1) in the Galician populationF Boán, J L CaeiroHuman Heredity|December 22, 2016
Meta-Analysis for Penalized Regression Methods with Multi-Cohort Genome-Wide Association StudiesChen Lu, George T O'Connor, Josée Dupuis, et al.Human Heredity|January 12, 2017
Biophysically Motivated Regulatory Network Inference: Progress and ProspectsTarmo Äijö, Richard BonneauHuman Heredity|January 1, 1987
Polymorphism of human red cell galactose-1-phosphate uridyl transferase in Serbia, YugoslaviaR Kovacević, V Kalimanovska, Z Jelić-Ivanović, et al.Human Heredity|August 2, 2003
Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort StudyDaniel O Stram, Christopher A Haiman, Joel N Hirschhorn, et al.Human Heredity|August 2, 2003
Pleiotropy and heterogeneity in the expression of atherogenic lipoproteins: the IRAS Family StudyJohn E Hokanson, Carl D Langefeld, Braxton D Mitchell, et al.Human Heredity|August 2, 2003
Sex-specific mutation rates for x-linked disorders: estimation and applicationPamela Flodman, Susan E HodgeHuman Heredity|August 2, 2003
Estimation and tests of haplotype-environment interaction when linkage phase is ambiguousS L Lake, H Lyon, K Tantisira, et al.Human Heredity|August 2, 2003
FLJ14813 missense mutation: a candidate for autosomal dominant thrombocytopenia on human chromosome 10Manish J Gandhi, Carrie L Cummings, Jonathan G DrachmanPageof 237