APA (7th ed.) Citation

Xing, X., Zeng, Z., Wang, Y., Pan, B., & Huang, X. (2024). Identification of potential molecular mechanism related to craniofacial dysmorphism caused by FOXI3 deficiency. Molecular Genetics & Genomic Medicine, 12(3), 1. https://doi.org/10.1002/mgg3.2411

Chicago Style (17th ed.) Citation

Xing, Xiao‐Liang, Ziqiang Zeng, Yana Wang, Bo Pan, and Xueshuang Huang. "Identification of Potential Molecular Mechanism Related to Craniofacial Dysmorphism Caused by FOXI3 Deficiency." Molecular Genetics & Genomic Medicine 12, no. 3 (2024): 1. https://doi.org/10.1002/mgg3.2411.

MLA (9th ed.) Citation

Xing, Xiao‐Liang, et al. "Identification of Potential Molecular Mechanism Related to Craniofacial Dysmorphism Caused by FOXI3 Deficiency." Molecular Genetics & Genomic Medicine, vol. 12, no. 3, 2024, p. 1, https://doi.org/10.1002/mgg3.2411.