Mapping of a single locus capable of complementing the defective heterochromatin phenotype of Roberts syndrome cells

MLA

McDaniel, Lisa D., et al. “Mapping of a Single Locus Capable of Complementing the Defective Heterochromatin Phenotype of Roberts Syndrome Cells.” American Journal of Human Genetics, vol. 77, no. 1, July 2005, p. 132. 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.133684676&authtype=sso&custid=ns315887.

APA

McDaniel, L. D., Tomkins, D. J., Stanbridge, E. J., Somerville, M. J., Friedberg, E. C., & Schultz, R. A. (2005). Mapping of a single locus capable of complementing the defective heterochromatin phenotype of Roberts syndrome cells. American Journal of Human Genetics, 77(1), 132.

Chicago

McDaniel, Lisa D., Darrell J. Tomkins, Eric J. Stanbridge, Martin J. Somerville, Errol C. Friedberg, and Roger A. Schultz. 2005. “Mapping of a Single Locus Capable of Complementing the Defective Heterochromatin Phenotype of Roberts Syndrome Cells.” American Journal of Human Genetics 77 (1): 132. 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.133684676&authtype=sso&custid=ns315887.