ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison

MLA

Richard J. A. Wilson, et al. “ROHHAD and Prader-Willi Syndrome (PWS): Clinical and Genetic Comparison.” Orphanet Journal of Rare Diseases, vol. 13, July 2018. 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.....5430aa29395db50a3465d7e8bf892971&authtype=sso&custid=ns315887.

APA

Richard J. A. Wilson, Sarah F. Barclay, N. Torben Bech-Hansen, Casey M. Rand, Rachel Wevrick, William T. Gibson, Lisa Nguyen, & Debra E. Weese-Mayer. (2018). ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison. Orphanet Journal of Rare Diseases, 13.

Chicago

Richard J. A. Wilson, Sarah F. Barclay, N. Torben Bech-Hansen, Casey M. Rand, Rachel Wevrick, William T. Gibson, Lisa Nguyen, and Debra E. Weese-Mayer. 2018. “ROHHAD and Prader-Willi Syndrome (PWS): Clinical and Genetic Comparison.” Orphanet Journal of Rare Diseases 13 (July). 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.....5430aa29395db50a3465d7e8bf892971&authtype=sso&custid=ns315887.