[Contiguous gene deletion syndrome in Xp21: the association between glycerol kinase deficiency, congenital suprarenal hypoplasia and Duchenne's muscular dystrophy].

MLA

Pantoja-Martínez, J., et al. “[Contiguous Gene Deletion Syndrome in Xp21: The Association between Glycerol Kinase Deficiency, Congenital Suprarenal Hypoplasia and Duchenne’s Muscular Dystrophy].” Revista de Neurologia, vol. 44, no. 10, May 2007, pp. 606–09. 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=17523119&authtype=sso&custid=ns315887.

APA

Pantoja-Martínez, J., Martínez-Castellano, F., Tarazona-Casany, I., Buesa-Ibáñez, E., Ardid-Encinar, M., Esparza-Sánchez, M. A., & Bonet-Arzo, J. (2007). [Contiguous gene deletion syndrome in Xp21: the association between glycerol kinase deficiency, congenital suprarenal hypoplasia and Duchenne’s muscular dystrophy]. Revista de Neurologia, 44(10), 606–609.

Chicago

Pantoja-Martínez, J, F Martínez-Castellano, I Tarazona-Casany, E Buesa-Ibáñez, M Ardid-Encinar, M A Esparza-Sánchez, and J Bonet-Arzo. 2007. “[Contiguous Gene Deletion Syndrome in Xp21: The Association between Glycerol Kinase Deficiency, Congenital Suprarenal Hypoplasia and Duchenne’s Muscular Dystrophy].” Revista de Neurologia 44 (10): 606–9. 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=17523119&authtype=sso&custid=ns315887.