Newborn screening for Prader–Willi syndrome is feasible: Early diagnosis for better outcomes.

MLA

Mahmoud, Ranim, et al. “Newborn Screening for Prader–Willi Syndrome Is Feasible: Early Diagnosis for Better Outcomes.” American Journal of Medical Genetics. Part A, vol. 179, no. 1, Jan. 2019, pp. 29–36. EBSCOhost, https://doi.org/10.1002/ajmg.a.60681.

APA

Mahmoud, R., Singh, P., Weiss, L., Lakatos, A., Oakes, M., Hossain, W., Butler, M. G., & Kimonis, V. (2019). Newborn screening for Prader–Willi syndrome is feasible: Early diagnosis for better outcomes. American Journal of Medical Genetics. Part A, 179(1), 29–36. https://doi.org/10.1002/ajmg.a.60681

Chicago

Mahmoud, Ranim, Preeti Singh, Lan Weiss, Anita Lakatos, Melanie Oakes, Waheeda Hossain, Merlin G. Butler, and Virginia Kimonis. 2019. “Newborn Screening for Prader–Willi Syndrome Is Feasible: Early Diagnosis for Better Outcomes.” American Journal of Medical Genetics. Part A 179 (1): 29–36. doi:10.1002/ajmg.a.60681.