The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats

MLA

Barbouti, Aikaterini, et al. “The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.” American Journal of Human Genetics, vol. 74, no. 1, Jan. 2004, p. 1. 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.112794444&authtype=sso&custid=ns315887.

APA

Barbouti, A., Stankiewicz, P., Nusbaum, C., Cuomo, C., Cook, A., Hoglund, M., Johansson, B., Hagemeijer, A., Park, S.-S., Mitelman, F., Lupski, J. R., & Fioretos, T. (2004). The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats. American Journal of Human Genetics, 74(1), 1.

Chicago

Barbouti, Aikaterini, Pawel Stankiewicz, Chad Nusbaum, Christina Cuomo, April Cook, Mattias Hoglund, Bertil Johansson, et al. 2004. “The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.” American Journal of Human Genetics 74 (1): 1. 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.112794444&authtype=sso&custid=ns315887.