Cite
Attenuated Phenotype in a Patient with Prader-Willi Syndrome and Duplication 16P11.2 Detected by Chromosomal Microarray
MLA
Vidit Bhargava, et al. “Attenuated Phenotype in a Patient with Prader-Willi Syndrome and Duplication 16P11.2 Detected by Chromosomal Microarray.” AACE Clinical Case Reports, vol. 2, no. 4, Jan. 2016. 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.doi.dedup.....2bc311388b209a605a54af8c161b917c&authtype=sso&custid=ns315887.
APA
Vidit Bhargava, Fadeke T. Adewole, Phillip D.K. Lee, & Sally S. Robinson. (2016). Attenuated Phenotype in a Patient with Prader-Willi Syndrome and Duplication 16P11.2 Detected by Chromosomal Microarray. AACE Clinical Case Reports, 2(4).
Chicago
Vidit Bhargava, Fadeke T. Adewole, Phillip D.K. Lee, and Sally S. Robinson. 2016. “Attenuated Phenotype in a Patient with Prader-Willi Syndrome and Duplication 16P11.2 Detected by Chromosomal Microarray.” AACE Clinical Case Reports 2 (4). 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.doi.dedup.....2bc311388b209a605a54af8c161b917c&authtype=sso&custid=ns315887.