APA (7th ed.) Citation

Zhong, W., Zhao, H., Huang, W., Zhang, M., Zhang, Q., Zhang, Y., . . . Lin, J. (2021). Identification of rare PTCH1 nonsense variant causing orofacial cleft in a Chinese family and an up-to-date genotype-phenotype analysis. Genes and Diseases, 8(5), 689. https://doi.org/10.1016/j.gendis.2019.12.010

Chicago Style (17th ed.) Citation

Zhong, Wenjie, et al. "Identification of Rare PTCH1 Nonsense Variant Causing Orofacial Cleft in a Chinese Family and an Up-to-date Genotype-phenotype Analysis." Genes and Diseases 8, no. 5 (2021): 689. https://doi.org/10.1016/j.gendis.2019.12.010.

MLA (9th ed.) Citation

Zhong, Wenjie, et al. "Identification of Rare PTCH1 Nonsense Variant Causing Orofacial Cleft in a Chinese Family and an Up-to-date Genotype-phenotype Analysis." Genes and Diseases, vol. 8, no. 5, 2021, p. 689, https://doi.org/10.1016/j.gendis.2019.12.010.