De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders.

MLA

Guo, Yicheng, et al. “De Novo Variants in Congenital Diaphragmatic Hernia Identify MYRF as a New Syndrome and Reveal Genetic Overlaps with Other Developmental Disorders.” PLoS Genetics, vol. 14, no. 12, Dec. 2018, pp. 1–26. EBSCOhost, https://doi.org/10.1371/journal.pgen.1007822.

APA

Guo, Y., Qi, H., Zhou, X., Zhu, N., Zhao, H., Kitaygorodsky, A., Shen, Y., Warner, B. W., Mychaliska, G. B., Potoka, D., Wagner, A. J., ElFiky, M., Wilson, J. M., High, F. A., Longoni, M., Donahoe, P. K., Nickerson, D., Bamshad, M., Yu, L., & Wynn, J. (2018). De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders. PLoS Genetics, 14(12), 1–26. https://doi.org/10.1371/journal.pgen.1007822

Chicago

Guo, Yicheng, Hongjian Qi, Xueya Zhou, Na Zhu, Haoquan Zhao, Alexander Kitaygorodsky, Yufeng Shen, et al. 2018. “De Novo Variants in Congenital Diaphragmatic Hernia Identify MYRF as a New Syndrome and Reveal Genetic Overlaps with Other Developmental Disorders.” PLoS Genetics 14 (12): 1–26. doi:10.1371/journal.pgen.1007822.