APA (7th ed.) Citation

G, R., AE, T., C, C., A, W., P, K., T, C., . . . GM, M. (2018). Bi-allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalus. American journal of medical genetics. Part A, 176(3), 676. https://doi.org/10.1002/ajmg.a.38592

Chicago Style (17th ed.) Citation

G, Ruggeri, Timms AE, Cheng C, Weiss A, Kollros P, Chapman T, Tully H, and Mirzaa GM. "Bi-allelic Mutations of CCDC88C Are a Rare Cause of Severe Congenital Hydrocephalus." American Journal of Medical Genetics. Part A 176, no. 3 (2018): 676. https://doi.org/10.1002/ajmg.a.38592.

MLA (9th ed.) Citation

G, Ruggeri, et al. "Bi-allelic Mutations of CCDC88C Are a Rare Cause of Severe Congenital Hydrocephalus." American Journal of Medical Genetics. Part A, vol. 176, no. 3, 2018, p. 676, https://doi.org/10.1002/ajmg.a.38592.