A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report.

MLA

Ng, Vivian Kwun Sin, et al. “A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report.” Diagnostics (Basel, Switzerland), vol. 11, no. 9, Aug. 2021. EBSCOhost, https://doi.org/10.3390/diagnostics11091576.

APA

Ng, V. K. S., Lau, T. K., Kan, A. S. Y., Chung, B. H. Y., Luk, H. M., Ng, W. F., Shi, M., Choy, K. W., Cao, Y., & Leung, W. C. (2021). A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report. Diagnostics (Basel, Switzerland), 11(9). https://doi.org/10.3390/diagnostics11091576

Chicago

Ng, Vivian Kwun Sin, Tze Kin Lau, Anita Sik Yau Kan, Brian Hon Yin Chung, Ho Ming Luk, Wai Fu Ng, Mengmeng Shi, Kwong Wai Choy, Ye Cao, and Wing Cheong Leung. 2021. “A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report.” Diagnostics (Basel, Switzerland) 11 (9). doi:10.3390/diagnostics11091576.