Absence of genetic linkage of CharcotMarieTooth disease HMSN Ia with chromosome 1 gene markers

MLA

Raeymaekers, P., et al. “Absence of Genetic Linkage of CharcotMarieTooth Disease HMSN Ia with Chromosome 1 Gene Markers.” Neurology (Ovid), vol. 39, no. 6, June 1989, pp. 844–46. 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=edo&AN=ejs49034974&authtype=sso&custid=ns315887.

APA

Raeymaekers, P., De Jonghe, P., Backhovens, H., Wehnert, A., De Winter, G., Swerts, L., Gheuens, J., Martin, J.-J., Vandenberghe, A., & Van Broeckhoven, C. (1989). Absence of genetic linkage of CharcotMarieTooth disease HMSN Ia with chromosome 1 gene markers. Neurology (Ovid), 39(6), 844–846.

Chicago

Raeymaekers, P., P. De Jonghe, H. Backhovens, A. Wehnert, G. De Winter, L. Swerts, J. Gheuens, J.-J. Martin, A. Vandenberghe, and C. Van Broeckhoven. 1989. “Absence of Genetic Linkage of CharcotMarieTooth Disease HMSN Ia with Chromosome 1 Gene Markers.” Neurology (Ovid) 39 (6): 844–46. 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=edo&AN=ejs49034974&authtype=sso&custid=ns315887.