N, S., P, E., B, K. P., C, P., & J, L. (2017). Acute pain in adolescents and young adults with sickle cell disease: Delayed and increased opioid dosing following transition to adult care. American journal of hematology, 92(4), E40. https://doi.org/10.1002/ajh.24647
Chicago Style (17th ed.) CitationN, Stehouwer, Edge P, Katie Park B, Piccone C, and Little J. "Acute Pain in Adolescents and Young Adults with Sickle Cell Disease: Delayed and Increased Opioid Dosing Following Transition to Adult Care." American Journal of Hematology 92, no. 4 (2017): E40. https://doi.org/10.1002/ajh.24647.
MLA (9th ed.) CitationN, Stehouwer, et al. "Acute Pain in Adolescents and Young Adults with Sickle Cell Disease: Delayed and Increased Opioid Dosing Following Transition to Adult Care." American Journal of Hematology, vol. 92, no. 4, 2017, p. E40, https://doi.org/10.1002/ajh.24647.