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文章标题：A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk.

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简介:A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk.
Antonacci F, Kidd J, Marques-Bonet T, Teague B, Ventura M, Girirajan S, Alkan C, Campbell C, Vives L, Malig M, Rosenfeld J, Ballif B, Shaffer L, Graves T, Wilson R, Schwartz D, and Eichler E.
Nature genetics
 42 (9), 745-750.Sep 2010