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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

C. Fernandez-Rozadilla; J. B. Cazier; I. Tomlinson; A. Brea-Fernández; M. J. Lamas; M. Baiget; L. A. López-Fernández; J. Clofent; L. Bujanda; D. Gonzalez; L. de Castro; K. Hemminki; X. Bessa; M. Andreu; R. Jover; R. Xicola; X. Llor; V. Moreno; A. Castells; S. Castellví-Bel; A. Carracedo; C. Ruiz-Ponte
Human Genetics · Vol. 133, Issue 5 · pp. 525-534 · 2014

Abstract

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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2014-05-01
Publication Year2014
Volume133
Issue5
Pages525-534
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-013-1390-4

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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