APA (7th ed.) Citation

Arce-Gonzalez, R., Chacon-Camacho, O. F., Navas-Perez, A., Gonzalez-Gonzalez, M. C., Martinez-Aguilar, A., & Zenteno, J. C. (2022). Novel CHRDL1 mutation causing X-linked megalocornea in a family with mild anterior segment manifestations in carrier females. Ophthalmic genetics, 43(2), 224-229. https://doi.org/10.1080/13816810.2021.2002917

Chicago Style (17th ed.) Citation

Arce-Gonzalez, Rocio, Oscar F. Chacon-Camacho, Alejandro Navas-Perez, María C. Gonzalez-Gonzalez, Alan Martinez-Aguilar, and Juan Carlos Zenteno. "Novel CHRDL1 Mutation Causing X-linked Megalocornea in a Family with Mild Anterior Segment Manifestations in Carrier Females." Ophthalmic Genetics 43, no. 2 (2022): 224-229. https://doi.org/10.1080/13816810.2021.2002917.

MLA (9th ed.) Citation

Arce-Gonzalez, Rocio, et al. "Novel CHRDL1 Mutation Causing X-linked Megalocornea in a Family with Mild Anterior Segment Manifestations in Carrier Females." Ophthalmic Genetics, vol. 43, no. 2, 2022, pp. 224-229, https://doi.org/10.1080/13816810.2021.2002917.