APA (7 ম সংস্করণ) উদ্ধৃতি

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.

শিকাগো স্টাইল (17 তম সংস্করণ) উদ্ধৃতি

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

M.L.A (9 ম সংস্করণ) উদ্ধৃতি

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