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A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk
Antonacci, Francesca, Kidd, Jeffrey M, Marques-Bonet, Tomas, Teague, Brian, Ventura, Mario, Girirajan, Santhosh, Alkan, Can, Campbell, Catarina D, Vives, Laura, Malig, MaikaVolume:
42
Year:
2010
Language:
english
Pages:
6
DOI:
10.1038/ng.643
File:
PDF, 1.05 MB
english, 2010