APA (7th ed.) Citation

Y, C., J, Q., Y, W., H, J., Y, J., M, J., . . . H, W. (2022). Genetic findings of Sanger and nanopore single-molecule sequencing in patients with X-linked hearing loss and incomplete partition type III. Orphanet journal of rare diseases, 17(1), 65. https://doi.org/10.1186/s13023-022-02235-7

Chicago Style (17th ed.) Citation

Y, Chen, et al. "Genetic Findings of Sanger and Nanopore Single-molecule Sequencing in Patients with X-linked Hearing Loss and Incomplete Partition Type III." Orphanet Journal of Rare Diseases 17, no. 1 (2022): 65. https://doi.org/10.1186/s13023-022-02235-7.

MLA (9th ed.) Citation

Y, Chen, et al. "Genetic Findings of Sanger and Nanopore Single-molecule Sequencing in Patients with X-linked Hearing Loss and Incomplete Partition Type III." Orphanet Journal of Rare Diseases, vol. 17, no. 1, 2022, p. 65, https://doi.org/10.1186/s13023-022-02235-7.