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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) Genomics Disorders.

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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:Genomics Disorders
Location:Wellcome Trust Sanger Institute, Hinxton, UK
UCL classification:UCL > School of Life and Medical Sciences > Faculty of Life Sciences > Biosciences (Division of) > Genetics, Evolution and Environment > UCL Genetics Institute

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