RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes.

MLA

Reijnders, Margot R. F., et al. “RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes.” American Journal of Human Genetics, vol. 101, no. 3, Sept. 2017, pp. 466–77. EBSCOhost, https://doi.org/10.1016/j.ajhg.2017.08.007.

APA

Reijnders, M. R. F., Ansor, N. M., Kousi, M., Yue, W. W., Tan, P. L., Clarkson, K., Clayton-Smith, J., Corning, K., Jones, J. R., Lam, W. W. K., Mancini, G. M. S., Marcelis, C., Mohammed, S., Pfundt, R., Roifman, M., Cohn, R., Chitayat, D., Millard, T. H., Katsanis, N., & Brunner, H. G. (2017). RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes. American Journal of Human Genetics, 101(3), 466–477. https://doi.org/10.1016/j.ajhg.2017.08.007

Chicago

Reijnders, Margot R.F., Nurhuda M. Ansor, Maria Kousi, Wyatt W. Yue, Perciliz L. Tan, Katie Clarkson, Jill Clayton-Smith, et al. 2017. “RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes.” American Journal of Human Genetics 101 (3): 466–77. doi:10.1016/j.ajhg.2017.08.007.