Lua APA (7ú heag.)

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

Lua i Stíl Chicago (17ú heag.)

O'Roak, B., et al. Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations. 2011.

Lua MLA (9ú heag.)

O'Roak, B., et al. Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations. 2011.

Rabhadh: Seans nach mbeach na luanna seo go hiomlán cruinn i ngach uile chás.