APA Alıntı

O’Roak, B. J., Deriziotis, P., Lee, C., Vives, L., Schwartz, J. J., Girirajan, S., . . . Eichler, E. E. (2011). Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.

Chicago Stili Alıntı

O’Roak, Brian J., et al. Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations. 2011.

MLA Alıntı

O’Roak, Brian J., et al. Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations. 2011.