APA

Babbs C., Lloyd D., Pagnamenta A. T., Twigg S. R. F., Green J., McGowan S. J., Mirza G., Naples R., Sharma V. P., Volpi E. V., Buckle V. J., Wall S. A., Knight S. J. L., Parr J. R. & Wilkie A. O. M. (20150619). De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder. : Journal of medical genetics.

Chicago

Babbs Christian, Lloyd Deborah, Pagnamenta Alistair T, Twigg Stephen R F, Green Joanne, McGowan Simon J, Mirza Ghazala, Naples Rebecca, Sharma Vikram P, Volpi Emanuela V, Buckle Veronica J, Wall Steven A, Knight Samantha J L, Parr Jeremy R and Wilkie Andrew O M. 20150619. De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder. : Journal of medical genetics.

Harvard

Babbs C., Lloyd D., Pagnamenta A. T., Twigg S. R. F., Green J., McGowan S. J., Mirza G., Naples R., Sharma V. P., Volpi E. V., Buckle V. J., Wall S. A., Knight S. J. L., Parr J. R. and Wilkie A. O. M. (20150619). De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder. : Journal of medical genetics.

MLA

Babbs Christian, Lloyd Deborah, Pagnamenta Alistair T, Twigg Stephen R F, Green Joanne, McGowan Simon J, Mirza Ghazala, Naples Rebecca, Sharma Vikram P, Volpi Emanuela V, Buckle Veronica J, Wall Steven A, Knight Samantha J L, Parr Jeremy R and Wilkie Andrew O M. De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder. : Journal of medical genetics. 20150619.