Works matching IS 00034800 AND DT 2003 AND VI 67 AND IP 2
Results: 10
Human Chromosome 17 in Essential Hypertension.
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- Annals of Human Genetics, 2003, v. 67, n. 2, p. 193, doi. 10.1046/j.1469-1809.2003.t01-1-00002.x
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- Article
A Note on the Optimal Measure of Allelic Association.
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- Annals of Human Genetics, 2003, v. 67, n. 2, p. 189, doi. 10.1046/j.1469-1809.2003.00025.x
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- Article
Using Affected Sibling Pairs to Distinguishing the Direct Effect of a Susceptibility Gene and the Indirect Effect of Linkage Disequilibrium.
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- Annals of Human Genetics, 2003, v. 67, n. 2, p. 185, doi. 10.1046/j.1469-1809.2003.00018.x
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- Article
Estimation of Multilocus Haplotype Effects Using Weighted Penalised Log-Likelihood: Analysis of Five Sequence Variations at the Cholesteryl Ester Transfer Protein Gene Locus.
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- Annals of Human Genetics, 2003, v. 67, n. 2, p. 175, doi. 10.1046/j.1469-1809.2003.00021.x
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Allowing for Genotyping Error in Analysis of Unmatched Case-Control Studies.
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- Annals of Human Genetics, 2003, v. 67, n. 2, p. 165, doi. 10.1046/j.1469-1809.2003.00020.x
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- Article
Maternal and Paternal Lineages of the Samaritan Isolate: Mutation Rates and Time to Most Recent Common Male Ancestor.
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- Annals of Human Genetics, 2003, v. 67, n. 2, p. 153, doi. 10.1046/j.1469-1809.2003.00024.x
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- Article
A Predominant European Ancestry of Paternal Lineages from Canary Islanders.
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- Annals of Human Genetics, 2003, v. 67, n. 2, p. 138, doi. 10.1046/j.1469-1809.2003.00015.x
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- Article
Segregation Analysis of Prostate Cancer in France: Evidence for Autosomal Dominant Inheritance and Residual Brother-brother Dependence.
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- Annals of Human Genetics, 2003, v. 67, n. 2, p. 125, doi. 10.1046/j.1469-1809.2003.00022.x
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Cladistic Analysis of Human Apolipoprotein A4 Polymorphisms in Relation to Quantitative Plasma Lipid Risk Factors of Coronary Heart Disease.
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- Annals of Human Genetics, 2003, v. 67, n. 2, p. 107, doi. 10.1046/j.1469-1809.2003.00023.x
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- Article
Family History is a Coronary Heart Disease Risk Factor in the Second Northwick Park Heart Study.
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- Annals of Human Genetics, 2003, v. 67, n. 2, p. 97, doi. 10.1046/j.1469-1809.2003.00017.x
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- Article