APA

Li F., Shen Y., Köhler U., Sharkey F. H., Menon D., Coulleaux L., Malan V., Rio M., McMullan D. J., Cox H., Fagan K. A., Gaunt L., Metcalfe K., Heinrich U., Hislop G., Maye U., Sutcliffe M., Wu B., Thiel B. D., Mulchandani S., Conlin L. K., Spinner N. B., Murphy K. M. & Batista D. A. S. (20100714). Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?. : European journal of medical genetics.

Chicago

Li Feng, Shen Yiping, Köhler Udo, Sharkey Freddie H, Menon Deepa, Coulleaux Laurence, Malan Valérie, Rio Marlène, McMullan Dominic J, Cox H, Fagan Kerry A, Gaunt Lorraine, Metcalfe Kay, Heinrich Uwe, Hislop Gordon, Maye Una, Sutcliffe Maxine, Wu Bai-Lin, Thiel Brian D, Mulchandani Surabhi, Conlin Laura K, Spinner Nancy B, Murphy Kathleen M and Batista Denise A S. 20100714. Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?. : European journal of medical genetics.

Harvard

Li F., Shen Y., Köhler U., Sharkey F. H., Menon D., Coulleaux L., Malan V., Rio M., McMullan D. J., Cox H., Fagan K. A., Gaunt L., Metcalfe K., Heinrich U., Hislop G., Maye U., Sutcliffe M., Wu B., Thiel B. D., Mulchandani S., Conlin L. K., Spinner N. B., Murphy K. M. and Batista D. A. S. (20100714). Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?. : European journal of medical genetics.

MLA

Li Feng, Shen Yiping, Köhler Udo, Sharkey Freddie H, Menon Deepa, Coulleaux Laurence, Malan Valérie, Rio Marlène, McMullan Dominic J, Cox H, Fagan Kerry A, Gaunt Lorraine, Metcalfe Kay, Heinrich Uwe, Hislop Gordon, Maye Una, Sutcliffe Maxine, Wu Bai-Lin, Thiel Brian D, Mulchandani Surabhi, Conlin Laura K, Spinner Nancy B, Murphy Kathleen M and Batista Denise A S. Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?. : European journal of medical genetics. 20100714.