APA (7th ed.) Citation

Y, W., Y, L., G, M., J, Z., Y, J., C, G., . . . Q, S. (2021). Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB. Human reproduction (Oxford, England), 36(10), 2793. https://doi.org/10.1093/humrep/deab185

Chicago Style (17th ed.) Citation

Y, Wu, et al. "Whole-exome Sequencing of Consanguineous Families with Infertile Men and Women Identifies Homologous Mutations in SPATA22 and MEIOB." Human Reproduction (Oxford, England) 36, no. 10 (2021): 2793. https://doi.org/10.1093/humrep/deab185.

MLA (9th ed.) Citation

Y, Wu, et al. "Whole-exome Sequencing of Consanguineous Families with Infertile Men and Women Identifies Homologous Mutations in SPATA22 and MEIOB." Human Reproduction (Oxford, England), vol. 36, no. 10, 2021, p. 2793, https://doi.org/10.1093/humrep/deab185.