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.
शिकागो शैली (17वां संस्करण) प्रशस्ति पत्रO'Roak, B., et al. Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations. 2011.
एमएलए (9वां संस्करण) प्रशस्ति पत्रO'Roak, B., et al. Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations. 2011.
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