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Oxford University Press

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Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease

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The allelic architecture of human disease genes: common disease–common variant… or not?

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Between tradition and innovation in new genetics: the continuity of medical pedigrees and the development of combination work in the case of Huntington's disease

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Association between Parkinson's disease and polymorphisms in the nNOS and iNOS genes in a community-based case–control study

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