DM, C., L, G., S, S., A, G., A, P., L, G., . . . E, F. (2013). Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype. American journal of medical genetics. Part A, 161A(2), 273. https://doi.org/10.1002/ajmg.a.35717
Chicago Style (17th ed.) CitationDM, Cordelli, et al. "Epilepsy in Mowat-Wilson Syndrome: Delineation of the Electroclinical Phenotype." American Journal of Medical Genetics. Part A 161A, no. 2 (2013): 273. https://doi.org/10.1002/ajmg.a.35717.
MLA (9th ed.) CitationDM, Cordelli, et al. "Epilepsy in Mowat-Wilson Syndrome: Delineation of the Electroclinical Phenotype." American Journal of Medical Genetics. Part A, vol. 161A, no. 2, 2013, p. 273, https://doi.org/10.1002/ajmg.a.35717.
Warning: These citations may not always be 100% accurate.