APA (7th ed.) Citation

Feng, Z., Chen, X., Li, T., Gao, H., Chen, W., Gao, Y., . . . Huang, G. (2022). An X-linked PLXNB3 mutation identified in patients with congenital heart disease with neurodevelopmental disabilities. Translational pediatrics, 11(11), 1852-1863. https://doi.org/10.21037/tp-22-556

Chicago Style (17th ed.) Citation

Feng, Zhiyu, et al. "An X-linked PLXNB3 Mutation Identified in Patients with Congenital Heart Disease with Neurodevelopmental Disabilities." Translational Pediatrics 11, no. 11 (2022): 1852-1863. https://doi.org/10.21037/tp-22-556.

MLA (9th ed.) Citation

Feng, Zhiyu, et al. "An X-linked PLXNB3 Mutation Identified in Patients with Congenital Heart Disease with Neurodevelopmental Disabilities." Translational Pediatrics, vol. 11, no. 11, 2022, pp. 1852-1863, https://doi.org/10.21037/tp-22-556.