Cite
A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation
MLA
Dreyer, Bo, et al. “A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation.” American Journal of Human Genetics, vol. 69, no. 1, July 2001, p. 228. 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.76996474&authtype=sso&custid=ns315887.
APA
Dreyer, B., Tranebjaerg, L., Brox, V., Rosenberg, T., Moller, C., Beneyto, M., Weston, M. D., Kimberling, W. J., & Nilssen, O. (2001). A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation. American Journal of Human Genetics, 69(1), 228.
Chicago
Dreyer, Bo, Lisbeth Tranebjaerg, Vigdis Brox, Thomas Rosenberg, Claes Moller, Magdalena Beneyto, Michael D. Weston, William J. Kimberling, and Oivind Nilssen. 2001. “A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation.” American Journal of Human Genetics 69 (1): 228. 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.76996474&authtype=sso&custid=ns315887.