A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer-Reference-Cited by-同舟云学术

A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer

Published:2013-11-12 Issue:5 Volume:133 Page:525-534
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Fernandez-Rozadilla C., ,Cazier J. B.,Tomlinson I.,Brea-Fernández A.,Lamas M. J.,Baiget M.,López-Fernández L. A.,Clofent J.,Bujanda L.,Gonzalez D.,de Castro L.,Hemminki K.,Bessa X.,Andreu M.,Jover R.,Xicola R.,Llor X.,Moreno V.,Castells A.,Castellví-Bel S.,Carracedo A.,Ruiz-Ponte C.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-013-1390-4.pdf

Reference40 articles.

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5. Dellinger AE, Saw SM, Goh LK, Seielstad M, Young TL, Li YJ (2010) Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays. Nucleic Acids Res 38:e105

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