APA aipamena

Antonacci, F., Kidd, J. M., Marques-Bonet, T., Teague, B., Ventura, M., Girirajan, S., . . . Eichler, E. E. (2010). A large, complex structural polymorphism at 16p12.1 underlies microdeletion disease risk.

Chicago Style aipamena

Antonacci, Francesca, et al. A Large, Complex Structural Polymorphism At 16p12.1 Underlies Microdeletion Disease Risk. 2010.

MLA aipamena

Antonacci, Francesca, et al. A Large, Complex Structural Polymorphism At 16p12.1 Underlies Microdeletion Disease Risk. 2010.