Application of full-genome analysis to diagnose rare monogenic disorders.

MLA

Shieh, Joseph T., et al. “Application of Full-Genome Analysis to Diagnose Rare Monogenic Disorders.” NPJ Genomic Medicine, 2021. 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=edsoai&AN=edsoai.on1287300150&authtype=sso&custid=ns315887.

APA

Shieh, J. T., Shieh, J. T., Penon-Portmann, M., Wong, K. H., Levy-Sakin, M., Verghese, M., Slavotinek, A., Gallagher, R. C., Mendelsohn, B. A., Tenney, J., Beleford, D., Perry, H., Chow, S. K., Sharo, A. G., Brenner, S. E., Qi, Z., Yu, J., Klein, O. D., Martin, D., … Boffelli, D. (2021). Application of full-genome analysis to diagnose rare monogenic disorders. NPJ Genomic Medicine.

Chicago

Shieh, Joseph T, Joseph T Shieh, Monica Penon-Portmann, Karen HY Wong, Michal Levy-Sakin, Michelle Verghese, Anne Slavotinek, et al. 2021. “Application of Full-Genome Analysis to Diagnose Rare Monogenic Disorders.” NPJ Genomic Medicine. 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=edsoai&AN=edsoai.on1287300150&authtype=sso&custid=ns315887.