[Clinical and molecular genetic features of 17alpha-hydroxylase deficiency: study of a case]

MLA

Ming-Hui, Yang, et al. “[Clinical and Molecular Genetic Features of 17alpha-Hydroxylase Deficiency: Study of a Case].” Zhonghua Yi Xue Za Zhi, vol. 86, no. 41, Feb. 2007. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.pmid..........e0d0407f067c36bd877510c7a022d65e&authtype=sso&custid=ns315887.

APA

Ming-Hui, Y., Xin-Bao, W., Ting, L., & Man-Yi, W. (2007). [Clinical and molecular genetic features of 17alpha-hydroxylase deficiency: study of a case]. Zhonghua Yi Xue Za Zhi, 86(41).

Chicago

Ming-Hui, Yang, Wu Xin-Bao, Li Ting, and Wang Man-Yi. 2007. “[Clinical and Molecular Genetic Features of 17alpha-Hydroxylase Deficiency: Study of a Case].” Zhonghua Yi Xue Za Zhi 86 (41). http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.pmid..........e0d0407f067c36bd877510c7a022d65e&authtype=sso&custid=ns315887.