APA-ийн эшлэл(7 дахь хэвлэлт)

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.

Чикаго-гийн эшлэл (17 дахь хэвлэлт)

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

MLA -ийн эшлэл (9 дэх хэвлэлт)

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