Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals-Reference-Cited by-同舟云学术

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

Published:2006-11-30 Issue:1 Volume:16 Page:1-14
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Simon-Sanchez Javier,Scholz Sonja,Fung Hon-Chung,Matarin Mar,Hernandez Dena,Gibbs J. Raphael,Britton Angela,de Vrieze Fabienne Wavrant,Peckham Elizabeth,Gwinn-Hardy Katrina,Crawley Anthony,Keen Judith C.,Nash Josefina,Borgaonkar Digamber,Hardy John,Singleton Andrew

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/16/1/1/17243500/ddl436.pdf

Reference19 articles.

1. Extended tracts of homozygosity in outbred human populations;Gibson;Hum. Mol. Genet.,2006

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

3. A high-resolution survey of deletion polymorphism in the human genome;Conrad;Nat. Genet.,2006

4. A genome-wide survey of structural variation between human and chimpanzee;Newman;Genome Res.,2005

5. Detection of chromosomal aberrations by a whole-genome microsatellite screen;Rosenberg;Am. J. Hum. Genet.,2000

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