APA (7th ed.) Citation

M, R., BHY, C., DM, R., R, T., N, M., LE, N., . . . D, C. (2021). Heterozygous NOTCH1 deletion associated with variable congenital heart defects. Clinical genetics, 99(6), 836. https://doi.org/10.1111/cge.13948

Chicago Style (17th ed.) Citation

M, Roifman, Chung BHY, Reid DM, Teitelbaum R, Martin N, Nield LE, Thompson M, Shannon P, and Chitayat D. "Heterozygous NOTCH1 Deletion Associated with Variable Congenital Heart Defects." Clinical Genetics 99, no. 6 (2021): 836. https://doi.org/10.1111/cge.13948.

MLA (9th ed.) Citation

M, Roifman, et al. "Heterozygous NOTCH1 Deletion Associated with Variable Congenital Heart Defects." Clinical Genetics, vol. 99, no. 6, 2021, p. 836, https://doi.org/10.1111/cge.13948.