Molecular characterization of the 22q13 deletion syndrome: comparison of over 50 cases

MLA

McDermid, H. E., et al. “Molecular Characterization of the 22q13 Deletion Syndrome: Comparison of over 50 Cases.” American Journal of Human Genetics, vol. 69, no. 4, Oct. 2001, p. 608. 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.78998038&authtype=sso&custid=ns315887.

APA

McDermid, H. E., Tse, W. Y., Stapleton, G. A., Artifoni, L., Dallapiccola, B., & Wilson, H. L. (2001). Molecular characterization of the 22q13 deletion syndrome: comparison of over 50 cases. American Journal of Human Genetics, 69(4), 608.

Chicago

McDermid, H.E., W.Y. Tse, G.A. Stapleton, L. Artifoni, B. Dallapiccola, and H.L. Wilson. 2001. “Molecular Characterization of the 22q13 Deletion Syndrome: Comparison of over 50 Cases.” American Journal of Human Genetics 69 (4): 608. 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.78998038&authtype=sso&custid=ns315887.