Cite
Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia
MLA
Callea, Michele, et al. Clinical and Molecular Study in a Family with Autosomal Dominant Hypohidrotic Ectodermal Dysplasia. Feb. 2017. 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.core.ac.uk....1419701145d5efba7fb746ce8a0397f6&authtype=sso&custid=ns315887.
APA
Callea, M., Cammarata-Scalisi, F., Willoughby, C. E., Giglio, S. R., Sani, I., Bargiacchi, S., Traficante, G., Bellacchio, E., Tadini, G., Yavuz, I., Galeotti, A., & Clarich, G. (2017). Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia.
Chicago
Callea, Michele, Francisco Cammarata-Scalisi, Colin E Willoughby, Sabrina R Giglio, Ilaria Sani, Sara Bargiacchi, Giovanna Traficante, et al. 2017. “Clinical and Molecular Study in a Family with Autosomal Dominant Hypohidrotic Ectodermal Dysplasia,” February. 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.core.ac.uk....1419701145d5efba7fb746ce8a0397f6&authtype=sso&custid=ns315887.