Human Heredity,volume 55,issue 1  (08-2003)

Period of time： 2003年1期

Publisher： Karger

Founded in： 1948

Total resources： 126

E-ISSN： 1423-0062|55|1

ISSN： 0001-5652

Subject： Q3 Genetics

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Human Heredity,volume 55,issue 1

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Mapping Quantitative Trait Loci Using Multiple Phenotypes in General Pedigrees

Human Heredity,volume 55,issue 1 , Vol. 55, Iss. 1, 2003-08 , pp. 1-15

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Linkage Analysis of Quantitative Trait Loci in the Presence of Heterogeneity

Human Heredity,volume 55,issue 1 , Vol. 55, Iss. 1, 2003-08 , pp. 16-26

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Erratum

Human Heredity,volume 55,issue 1 , Vol. 55, Iss. 1, 2003-08 , pp. 26-

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Choosing Haplotype-Tagging SNPS Based on Unphased Genotype Data Using a Preliminary Sample of Unrelated Subjects with an Example from the Multiethnic Cohort Study

Human Heredity,volume 55,issue 1 , Vol. 55, Iss. 1, 2003-08 , pp. 27-36

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Number of SNPS Loci Needed to Detect Population Structure

Human Heredity,volume 55,issue 1 , Vol. 55, Iss. 1, 2003-08 , pp. 37-45

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Pleiotropy and Heterogeneity in the Expression of Atherogenic Lipoproteins: The IRAS Family Study

Human Heredity,volume 55,issue 1 , Vol. 55, Iss. 1, 2003-08 , pp. 46-50

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Sex-Specific Mutation Rates for X-Linked Disorders: Estimation and Application

Human Heredity,volume 55,issue 1 , Vol. 55, Iss. 1, 2003-08 , pp. 51-55

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Estimation and Tests of Haplotype-Environment Interaction when Linkage Phase Is Ambiguous

Human Heredity,volume 55,issue 1 , Vol. 55, Iss. 1, 2003-08 , pp. 56-65

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FLJ14813 Missense Mutation: A Candidate for Autosomal Dominant Thrombocytopenia on Human Chromosome 10

Human Heredity,volume 55,issue 1 , Vol. 55, Iss. 1, 2003-08 , pp. 66-70

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Localization of A Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus (DFNB38) to 6q26-q27 in a Consanguineous Kindred from Pakistan

Human Heredity,volume 55,issue 1 , Vol. 55, Iss. 1, 2003-08 , pp. 71-74

Karger

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Total 10 item(s)