De novo loss-of-function variants in X-linked MED12are associated with Hardikar syndrome in females

MLA

Li, Dong, et al. “De Novo Loss-of-Function Variants in X-Linked MED12are Associated with Hardikar Syndrome in Females.” Genetics in Medicine, vol. 23, no. 4, Apr. 2021, pp. 637–44. EBSCOhost, https://doi.org/10.1038/s41436-020-01031-7.

APA

Li, D., Strong, A., Shen, K. M., Cassiman, D., Van Dyck, M., Linhares, N. D., Valadares, E. R., Wang, T., Pena, S. D. J., Jaeken, J., Vergano, S., Zackai, E., Hing, A., Chow, P., Ganguly, A., Scholz, T., Bierhals, T., Philipp, D., Hakonarson, H., & Bhoj, E. (2021). De novo loss-of-function variants in X-linked MED12are associated with Hardikar syndrome in females. Genetics in Medicine, 23(4), 637–644. https://doi.org/10.1038/s41436-020-01031-7

Chicago

Li, Dong, Alanna Strong, Kaitlyn M. Shen, David Cassiman, Maria Van Dyck, Natalia Duarte Linhares, Eugenia Ribeiro Valadares, et al. 2021. “De Novo Loss-of-Function Variants in X-Linked MED12are Associated with Hardikar Syndrome in Females.” Genetics in Medicine 23 (4): 637–44. doi:10.1038/s41436-020-01031-7.