APA

Simpson N. H., Ceroni F., Reader R. H., Covill L. E., Knight J. C., Hennessy E. R., Bolton P. F., Conti-Ramsden G., O'Hare A., Baird G., Fisher S. E. & Newbury D. F. (20160615). Genome-wide analysis identifies a role for common copy number variants in specific language impairment. : European journal of human genetics : EJHG.

Chicago

Simpson Nuala H, Ceroni Fabiola, Reader Rose H, Covill Laura E, Knight Julian C, Hennessy Elizabeth R, Bolton Patrick F, Conti-Ramsden Gina, O'Hare Anne, Baird Gillian, Fisher Simon E and Newbury Dianne F. 20160615. Genome-wide analysis identifies a role for common copy number variants in specific language impairment. : European journal of human genetics : EJHG.

Harvard

Simpson N. H., Ceroni F., Reader R. H., Covill L. E., Knight J. C., Hennessy E. R., Bolton P. F., Conti-Ramsden G., O'Hare A., Baird G., Fisher S. E. and Newbury D. F. (20160615). Genome-wide analysis identifies a role for common copy number variants in specific language impairment. : European journal of human genetics : EJHG.

MLA

Simpson Nuala H, Ceroni Fabiola, Reader Rose H, Covill Laura E, Knight Julian C, Hennessy Elizabeth R, Bolton Patrick F, Conti-Ramsden Gina, O'Hare Anne, Baird Gillian, Fisher Simon E and Newbury Dianne F. Genome-wide analysis identifies a role for common copy number variants in specific language impairment. : European journal of human genetics : EJHG. 20160615.