A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk
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author: Francesca Antonacci, Jeffrey M. Kidd, Tomas Marques-Bonet, Mario Ventura, Can Alkan, Evan E. Eichler, Maika Malig, Jill A Rosenfeld, Catarina D Campbell, Blake C Ballif, Santhosh Girirajan
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