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.
芝加哥风格引文Babbs, C., et al. De Novo and Rare Inherited Mutations Implicate the Transcriptional Coregulator TCF20/SPBP in Autism Spectrum Disorder. 2014.
MLA引文Babbs, C., et al. De Novo and Rare Inherited Mutations Implicate the Transcriptional Coregulator TCF20/SPBP in Autism Spectrum Disorder. 2014.
警告：这些引文格式不一定是100％准确.