Kanca, O., Andrews, J. C., Patel, C., Slavotinek, A. M., Williams, J., Indaram, M., . . . Malicdan, M. C. V. (2019). De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. American journal of human genetics, 105(2), 413-424. https://doi.org/10.1016/j.ajhg.2019.06.014
Chicago Style (17th ed.) CitationKanca, Oguz, et al. "De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia." American Journal of Human Genetics 105, no. 2 (2019): 413-424. https://doi.org/10.1016/j.ajhg.2019.06.014.
MLA (9th ed.) CitationKanca, Oguz, et al. "De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia." American Journal of Human Genetics, vol. 105, no. 2, 2019, pp. 413-424, https://doi.org/10.1016/j.ajhg.2019.06.014.