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.
Citace podle Chicago (17th ed.)Babbs, C., et al. De Novo and Rare Inherited Mutations Implicate the Transcriptional Coregulator TCF20/SPBP in Autism Spectrum Disorder. 2014.
Citace podle MLA (9th ed.)Babbs, C., et al. De Novo and Rare Inherited Mutations Implicate the Transcriptional Coregulator TCF20/SPBP in Autism Spectrum Disorder. 2014.
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