APA

Zarate Y. A., Perry H., Ben-Omran T., Sellars E. A., Stein Q., Almureikhi M., Simmons K., Klein O., Fish J., Feingold M., Douglas J., Kruer M. C., Si Y., Mao R., McKnight D., Gibellini F., Retterer K. & Slavotinek A. (20160108). Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing. : American journal of medical genetics. Part A.

Chicago

Zarate Yuri A, Perry Hazel, Ben-Omran Tawfeg, Sellars Elizabeth A, Stein Quinn, Almureikhi Mariam, Simmons Kirk, Klein Ophir, Fish Jennifer, Feingold Murray, Douglas Jessica, Kruer Michael C, Si Yue, Mao Rong, McKnight Dianalee, Gibellini Federica, Retterer Kyle and Slavotinek Anne. 20160108. Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing. : American journal of medical genetics. Part A.

Harvard

Zarate Y. A., Perry H., Ben-Omran T., Sellars E. A., Stein Q., Almureikhi M., Simmons K., Klein O., Fish J., Feingold M., Douglas J., Kruer M. C., Si Y., Mao R., McKnight D., Gibellini F., Retterer K. and Slavotinek A. (20160108). Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing. : American journal of medical genetics. Part A.

MLA

Zarate Yuri A, Perry Hazel, Ben-Omran Tawfeg, Sellars Elizabeth A, Stein Quinn, Almureikhi Mariam, Simmons Kirk, Klein Ophir, Fish Jennifer, Feingold Murray, Douglas Jessica, Kruer Michael C, Si Yue, Mao Rong, McKnight Dianalee, Gibellini Federica, Retterer Kyle and Slavotinek Anne. Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing. : American journal of medical genetics. Part A. 20160108.