Origins and functional impact of copy number variation in the human genome

Nature - Tập 464 Số 7289 - Trang 704-712 - 2010
Donald F. Conrad1, Dalila Pinto2, Richard Redon3,1, Lars Feuk2,4, Ömer Gökçümen5, Goo Jun1, Jan Aerts1, T. Daniel Andrews1, C. Barnes1, Peter J. Campbell1, Tomas Fitzgerald1, Min Hu1, Chun Hwa Ihm5, Kati Kristiansson1, Daniel G. MacArthur1, Jeffrey R. MacDonald2, Ifejinelo Onyiah1, Andy Wing Chun Pang2, Samuel C. Robson1, Kathy Stirrups1, Armand Valsesia1, Klaudia Walter1, John Wei2, Chris Tyler‐Smith1, Nigel P. Carter1, Charles Lee5, Stephen W. Scherer6,2, Matthew E. Hurles1
1, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK,
2The Centre for Applied Genomics and Program in Genetics and Genomic Biology, The Hospital for Sick Children, MaRS Centre–East Tower, 101 College Street, Room 14-701, Toronto, Ontario, M5G 1L7, Canada
3Inserm UMR915, L’institut du thorax, Nantes 44035, France ,
4Uppsala: Department of Genetics and Pathology, Rudbeck Laboratory Uppsala University, Uppsala 751 85, Sweden
5Department of Pathology, Brigham & Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115 USA
6Department of Molecular Genetics, University of Toronto, Toronto M5S 1A8, Canada

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