Cite
Epigenetic abnormalities associated with a chromosome 18(q21-q22)inversion and a Gilles de la Tourette syndrome phenotype
MLA
State, Matthew W., et al. “Epigenetic Abnormalities Associated with a Chromosome 18(Q21-Q22)Inversion and a Gilles de La Tourette Syndrome Phenotype.” Proceedings of the National Academy of Sciences of the United States, vol. 100, no. 8, Apr. 2003, p. 4684. 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.101176217&authtype=sso&custid=ns315887.
APA
State, M. W., Greally, J. M., Cuker, A., Bowers, P. N., Henegariu, O., Morgan, T. M., Gunel, M., DiLuna, M., King, R. A., Nelson, C., Donovan, A., Anderson, G. M., Leckman, J. F., Hawkins, T., Pauls, D. L., Lifton, R. P., & Ward, D. C. (2003). Epigenetic abnormalities associated with a chromosome 18(q21-q22)inversion and a Gilles de la Tourette syndrome phenotype. Proceedings of the National Academy of Sciences of the United States, 100(8), 4684.
Chicago
State, Matthew W., John M. Greally, Adam Cuker, Peter N. Bowers, Octavian Henegariu, Thomas M. Morgan, Murat Gunel, et al. 2003. “Epigenetic Abnormalities Associated with a Chromosome 18(Q21-Q22)Inversion and a Gilles de La Tourette Syndrome Phenotype.” Proceedings of the National Academy of Sciences of the United States 100 (8): 4684. 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.101176217&authtype=sso&custid=ns315887.