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A genome-wide copy number variant association study for eight common disorders in 16,000 cases and 3,000 controls

Plagnol, V; (2010) A genome-wide copy number variant association study for eight common disorders in 16,000 cases and 3,000 controls. In: (Proceedings) European Society of Human Genetics.

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Type: Proceedings paper
Title: A genome-wide copy number variant association study for eight common disorders in 16,000 cases and 3,000 controls
Event: European Society of Human Genetics
Location: Gotenborg, Sweden
UCL classification: UCL > School of Life and Medical Sciences > Faculty of Life Sciences > Biosciences (Division of) > Genetics, Evolution and Environment > UCL Genetics Institute
URI: http://discovery.ucl.ac.uk/id/eprint/1371167
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