Murray, M. F., Khoury, M. J., & Abul-Husn, N. S. (2022). Addressing the routine failure to clinically identify monogenic cases of common disease. Genome Medicine, 14(1), 1. https://doi.org/10.1186/s13073-022-01062-6
Chicago Style (17th ed.) CitationMurray, Michael F., Muin J. Khoury, and Noura S. Abul-Husn. "Addressing the Routine Failure to Clinically Identify Monogenic Cases of Common Disease." Genome Medicine 14, no. 1 (2022): 1. https://doi.org/10.1186/s13073-022-01062-6.
MLA (9th ed.) CitationMurray, Michael F., et al. "Addressing the Routine Failure to Clinically Identify Monogenic Cases of Common Disease." Genome Medicine, vol. 14, no. 1, 2022, p. 1, https://doi.org/10.1186/s13073-022-01062-6.
Warning: These citations may not always be 100% accurate.