APA (7th ed.) Citation

KD, K., L, G., M, P., E, Y., M, L., MM, A., . . . P, C. (2025). Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years. Genetics in medicine : official journal of the American College of Medical Genetics, 27(10), 101497. https://doi.org/10.1016/j.gim.2025.101497

Chicago Style (17th ed.) Citation

KD, Kernohan, et al. "Newborn Screening for Common Genetic Variants Associated with Permanent Hearing Loss: Implementation in Ontario and a Review of the First 3 Years." Genetics in Medicine : Official Journal of the American College of Medical Genetics 27, no. 10 (2025): 101497. https://doi.org/10.1016/j.gim.2025.101497.

MLA (9th ed.) Citation

KD, Kernohan, et al. "Newborn Screening for Common Genetic Variants Associated with Permanent Hearing Loss: Implementation in Ontario and a Review of the First 3 Years." Genetics in Medicine : Official Journal of the American College of Medical Genetics, vol. 27, no. 10, 2025, p. 101497, https://doi.org/10.1016/j.gim.2025.101497.