A large, complex structural polymorphism at 16p12.1 underlies microdeletion disease risk
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David C. Schwartz | Can Alkan | Evan E. Eichler | Brian Teague | Laura Vives | Francesca Antonacci | Santhosh Girirajan | Jill A. Rosenfeld | Mario Ventura | Jeffrey M. Kidd | Catarina D. Campbell | J. Rosenfeld | E. Eichler | M. Malig | F. Antonacci | T. Graves | C. Alkan | R. Wilson | L. Vives | L. Shaffer | J. Kidd | T. Marquès-Bonet | D. Schwartz | M. Ventura | S. Girirajan | B. Ballif | Richard K. Wilson | Tomas Marques-Bonet | Maika Malig | Blake C. Ballif | Lisa G. Shaffer | Tina A. Graves | Brian Teague | Laura Vives | Tomàs Marquès-Bonet | R. Wilson | Maika Malig | Tina Graves
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