Strategies in complex disease mapping

被引：86

作者：

Johnson, GCL ^{[1
]}

Todd, JA ^{[1
]}

机构：

[1] Univ Cambridge, Dept Med Genet, Wellcome Trust Ctr Mol Mechanisms Dis, Addenbrookes Hosp, Cambridge CB2 2XY, England

来源：

CURRENT OPINION IN GENETICS & DEVELOPMENT | 2000年 / 10卷 / 03期

基金：

英国惠康基金;

关键词：

D O I：

10.1016/S0959-437X(00)00075-7

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 [细胞生物学]; 090102 [作物遗传育种];

摘要：

Dissecting the genetics of common, complex disorders remains one of the great challenges in human genetics. The acceleration of human genome sequence determination, improvements in informatics, large-scale identification of single nucleotide polymorphisms and improvements in scoring technologies have now increased the feasibility of identifying polymorphisms that predispose to common disease.

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收藏

页码：330 / 334

页数：5

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