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

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Title: A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer.
Authors: Fernandez-Rozadilla, C., Cazier, J.1, Tomlinson, I., Brea-Fernández, A.2, Lamas, M.3, Baiget, M.4, López-Fernández, L.5, Clofent, J., Bujanda, L.6, Gonzalez, D.7, Castro, L.8, Hemminki, K., Bessa, X.9, Andreu, M.9, Jover, R.10, Xicola, R.11, Llor, X.11, Moreno, V.12, Castells, A.13, Castellví-Bel, S.13
Source: Human Genetics. May2014, Vol. 133 Issue 5, p525-534. 10p.
Database: Academic Search Ultimate
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  Data: <searchLink fieldCode="JN" term="%22Human+Genetics%22">Human Genetics</searchLink>. May2014, Vol. 133 Issue 5, p525-534. 10p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=95563022
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