APA (7th ed.) Citation

M, A. S., EB, F., JE, F., V, M., J, K., S, S., . . . SA, L. (2019). NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families. European journal of medical genetics, 62(3), 204. https://doi.org/10.1016/j.ejmg.2018.07.015

Chicago Style (17th ed.) Citation

M, Al Shehhi, et al. "NRXN1 Deletion Syndrome; Phenotypic and Penetrance Data from 34 Families." European Journal of Medical Genetics 62, no. 3 (2019): 204. https://doi.org/10.1016/j.ejmg.2018.07.015.

MLA (9th ed.) Citation

M, Al Shehhi, et al. "NRXN1 Deletion Syndrome; Phenotypic and Penetrance Data from 34 Families." European Journal of Medical Genetics, vol. 62, no. 3, 2019, p. 204, https://doi.org/10.1016/j.ejmg.2018.07.015.