Cite
Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse-Sakati Syndrome: Report of a Family with Mutation in theC2orf37Gene
MLA
B S Nina Ishorst, et al. “Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse-Sakati Syndrome: Report of a Family with Mutation in TheC2orf37Gene.” Pediatric Dermatology, vol. 31, Sept. 2013, pp. 83–87. 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.....c4f66ae5d553d742a5332d0147f15076&authtype=sso&custid=ns315887.
APA
B S Nina Ishorst, Sandra M. Pasternack, Ramon Grimalt, Hassnaa Mahmoudi, Regina C. Betz, & Arti Nanda. (2013). Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse-Sakati Syndrome: Report of a Family with Mutation in theC2orf37Gene. Pediatric Dermatology, 31, 83–87.
Chicago
B S Nina Ishorst, Sandra M. Pasternack, Ramon Grimalt, Hassnaa Mahmoudi, Regina C. Betz, and Arti Nanda. 2013. “Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse-Sakati Syndrome: Report of a Family with Mutation in TheC2orf37Gene.” Pediatric Dermatology 31 (September): 83–87. 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.....c4f66ae5d553d742a5332d0147f15076&authtype=sso&custid=ns315887.