Cite
NF1 microdeletion syndrome: a phenotypical characterization of a rare case of neurofibromatosis type 1.
MLA
Lopes, Jorge, et al. “NF1 Microdeletion Syndrome: A Phenotypical Characterization of a Rare Case of Neurofibromatosis Type 1.” Acta Dermatovenerologica Alpina, Pannonica, et Adriatica, vol. 29, no. 2, June 2020, pp. 85–87. 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=cmedm&AN=32566957&authtype=sso&custid=ns315887.
APA
Lopes, J., Teixeira, D., Sousa, C., Baptista, A., & Osório Ferreira, E. (2020). NF1 microdeletion syndrome: a phenotypical characterization of a rare case of neurofibromatosis type 1. Acta Dermatovenerologica Alpina, Pannonica, et Adriatica, 29(2), 85–87.
Chicago
Lopes, Jorge, Diogo Teixeira, Cristina Sousa, Armando Baptista, and Eduarda Osório Ferreira. 2020. “NF1 Microdeletion Syndrome: A Phenotypical Characterization of a Rare Case of Neurofibromatosis Type 1.” Acta Dermatovenerologica Alpina, Pannonica, et Adriatica 29 (2): 85–87. 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=cmedm&AN=32566957&authtype=sso&custid=ns315887.