Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases-Reference-Cited by-同舟云学术

Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases

Published:2007-07-31 Issue:23 Volume:16 Page:2783-2794
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

de Smith Adam J.,Tsalenko Anya,Sampas Nick,Scheffer Alicia,Yamada N. Alice,Tsang Peter,Ben-Dor Amir,Yakhini Zohar,Ellis Richard J.,Bruhn Laurakay,Laderman Stephen,Froguel Philippe,Blakemore Alexandra I.F.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/16/23/2783/17244006/ddm208.pdf

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4. Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome;Locke;Am. J. Hum. Genet.,2006

5. Common deletion polymorphisms in the human genome;McCarroll;Nat. Genet.,2006

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