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.
Citación estilo ChicagoO'Roak, B., et al. Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations. 2011.
Cita MLAO'Roak, B., et al. Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations. 2011.
Warning: These citations may not always be 100% accurate.