Ethics watch - Implications of copy-number variation in the human genome: A time for questions

被引：10

作者：

Daar, AS

Scherer, SW

Hegele, RA

机构：

[1] Univ Toronto, Dept Publ Hlth Sci, Toronto, ON, Canada

[2] Univ Toronto, Dept Surg, Toronto, ON, Canada

[3] Univ Toronto, McLaughlin Ctr Mol Med, Toronto, ON, Canada

[4] Hosp Sick Children, Program Genet & Genom Biol, Toronto, ON M5G 1X8, Canada

[5] Hosp Sick Children, Ctr Appl Genom, Toronto, ON M5G 1X8, Canada

[6] Univ Toronto, Dept Mol & Med Genet, Toronto, ON, Canada

[7] Univ Western Ontario, Blackburn Cardiovasc Genet Lab, Robarts Res Inst, London, ON N6A 3K7, Canada

[8] Univ Western Ontario, Schulich Sch Med & Dent, London, ON N6A 3K7, Canada

来源：

NATURE REVIEWS GENETICS | 2006年 / 7卷 / 06期

关键词：

D O I：

10.1038/nrg1884

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：414 / 414

页数：1

共 5 条

[1] Human genome: Patchwork people [J].

Check, E .

NATURE, 2005, 437 (7062) :1084-1086

[2] Pharmacogenetics and geographical ancestry: implications for drug development and global health [J].

Daar, AS ;

Singer, PA .

NATURE REVIEWS GENETICS, 2005, 6 (03) :241-246

[3] Structural variation in the human genome [J].

Feuk, L ;

Carson, AR ;

Scherer, SW .

NATURE REVIEWS GENETICS, 2006, 7 (02) :85-97

[4] Vive la difference! [J].

Lee, C .

NATURE GENETICS, 2005, 37 (07) :660-661

[5] Changing the paradigm from 'race' to human genome variation [J].

Royal, CDM ;

Dunston, GM .

NATURE GENETICS, 2004, 36 (11) :S5-S7

← 1 →