Systemic hyalinosis: a distinctive early childhood-onset disorder characterized by mutations in the anthrax toxin receptor 2 gene (ANTRX2)

MLA

Shieh, Joseph T. C., et al. “Systemic Hyalinosis: A Distinctive Early Childhood-Onset Disorder Characterized by Mutations in the Anthrax Toxin Receptor 2 Gene (ANTRX2).” Pediatrics, vol. 118, no. 5, Nov. 2006, p. 2210. 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=edsggo&AN=edsgcl.155023718&authtype=sso&custid=ns315887.

APA

Shieh, J. T. C., Swidler, P., Martignetti, J. A., Ramirez, M. C. M., Balboni, I., Kaplan, J., Kennedy, J., Omar, A.-R., Enns, G. M., Sandborg, C., Slavotinek, A., & Hoyme, H. E. (2006). Systemic hyalinosis: a distinctive early childhood-onset disorder characterized by mutations in the anthrax toxin receptor 2 gene (ANTRX2). Pediatrics, 118(5), 2210.

Chicago

Shieh, Joseph T.C., Petra Swidler, John A. Martignetti, Maria Celeste M. Ramirez, Imelda Balboni, Julie Kaplan, Jeanette Kennedy, et al. 2006. “Systemic Hyalinosis: A Distinctive Early Childhood-Onset Disorder Characterized by Mutations in the Anthrax Toxin Receptor 2 Gene (ANTRX2).” Pediatrics 118 (5): 2210. 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=edsggo&AN=edsgcl.155023718&authtype=sso&custid=ns315887.