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.
Chicago-referens (17:e uppl.)O'Roak, B., et al. Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations. 2011.
MLA-referens (9:e uppl.)O'Roak, B., et al. Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations. 2011.
Varning: dessa hänvisningar är inte alltid fullständigt riktiga.