APA (7th ed.) Citation

Williams, A., Divin, K., Burrage, L. C., Craigen, W. J., Scaglia, F., Soler‐Alfonso, C., . . . Marom, R. (2026). Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency. American Journal of Medical Genetics. Part A, 200(8), 1814. https://doi.org/10.1002/ajmg.a.70154

Chicago Style (17th ed.) Citation

Williams, Aaron, Kristian Divin, Lindsay C. Burrage, William J. Craigen, Fernando Scaglia, Claudia Soler‐Alfonso, V. Reid Sutton, Kevin E. Glinton, and Ronit Marom. "Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency." American Journal of Medical Genetics. Part A 200, no. 8 (2026): 1814. https://doi.org/10.1002/ajmg.a.70154.

MLA (9th ed.) Citation

Williams, Aaron, et al. "Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency." American Journal of Medical Genetics. Part A, vol. 200, no. 8, 2026, p. 1814, https://doi.org/10.1002/ajmg.a.70154.