APA (7th ed.) Citation

Yang, K., Wang, X., Wang, W., Han, M., Hu, L., Kang, D., . . . Xu, J. (2023). A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4. Molecular Genetics & Genomic Medicine, 11(3), 1. https://doi.org/10.1002/mgg3.2103

Chicago Style (17th ed.) Citation

Yang, Kun, et al. "A Newborn Male with Myhre Syndrome, Hearing Loss, and Complete Syndactyly of Fingers 3–4." Molecular Genetics & Genomic Medicine 11, no. 3 (2023): 1. https://doi.org/10.1002/mgg3.2103.

MLA (9th ed.) Citation

Yang, Kun, et al. "A Newborn Male with Myhre Syndrome, Hearing Loss, and Complete Syndactyly of Fingers 3–4." Molecular Genetics & Genomic Medicine, vol. 11, no. 3, 2023, p. 1, https://doi.org/10.1002/mgg3.2103.