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 Style (17th ed.) CitationO'Roak, B., et al. Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations. 2011.
MLA citiranjeO'Roak, B., et al. Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations. 2011.
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