APA (7th ed.) Citation

ES, C., A, H., IN, M., M, E., S, M., A, Y., . . . MC, M. (2019). Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556. Neurogenetics, 20(2), 91. https://doi.org/10.1007/s10048-019-00577-2

Chicago Style (17th ed.) Citation

ES, Cauley, et al. "Overlap of Polymicrogyria, Hydrocephalus, and Joubert Syndrome in a Family with Novel Truncating Mutations in ADGRG1/GPR56 and KIAA0556." Neurogenetics 20, no. 2 (2019): 91. https://doi.org/10.1007/s10048-019-00577-2.

MLA (9th ed.) Citation

ES, Cauley, et al. "Overlap of Polymicrogyria, Hydrocephalus, and Joubert Syndrome in a Family with Novel Truncating Mutations in ADGRG1/GPR56 and KIAA0556." Neurogenetics, vol. 20, no. 2, 2019, p. 91, https://doi.org/10.1007/s10048-019-00577-2.