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A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk

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Description scientific article
Author/s

author: Mario Ventura  Tomas Marques-Bonet  Jill A Rosenfeld  Blake C Ballif  Jeffrey M. Kidd  Catarina D Campbell  Maika Malig  Francesca Antonacci  Can Alkan  Evan E. Eichler  Santhosh Girirajan 

Publication date August 22, 2010
Language English
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