Li, X., Shi, W., Ding, X., Li, J., Li, Y., Wu, J., . . . Zhu, M. (2022). Identification of a novel TBX5 mutation in a Chinese family with rare symptoms of Holt–Oram syndrome. Elsevier.
Chicago Style (17th ed.) CitationLi, Xia, et al. Identification of a Novel TBX5 Mutation in a Chinese Family with Rare Symptoms of Holt–Oram Syndrome. Elsevier, 2022.
MLA (9th ed.) CitationLi, Xia, et al. Identification of a Novel TBX5 Mutation in a Chinese Family with Rare Symptoms of Holt–Oram Syndrome. Elsevier, 2022.
Warning: These citations may not always be 100% accurate.