Cita APA (7a ed.)

Babbs, C., Lloyd, D., Pagnamenta, A., Twigg, S., Green, J., McGowan, S., . . . Wilkie, A. (2014). De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.

Cita Chicago Style (17a ed.)

Babbs, C., et al. De Novo and Rare Inherited Mutations Implicate the Transcriptional Coregulator TCF20/SPBP in Autism Spectrum Disorder. 2014.

Cita MLA (9a ed.)

Babbs, C., et al. De Novo and Rare Inherited Mutations Implicate the Transcriptional Coregulator TCF20/SPBP in Autism Spectrum Disorder. 2014.