APA (7th ed.) Citation

Zhou, J., Zheng, Y., Liang, G., Xu, X., Liu, J., Chen, S., . . . Chen, J. (2022). Atypical deletion of Williams–Beuren syndrome reveals the mechanism of neurodevelopmental disorders. BMC Medical Genomics, 15, 1. https://doi.org/10.1186/s12920-022-01227-7

Chicago Style (17th ed.) Citation

Zhou, Jianrong, et al. "Atypical Deletion of Williams–Beuren Syndrome Reveals the Mechanism of Neurodevelopmental Disorders." BMC Medical Genomics 15 (2022): 1. https://doi.org/10.1186/s12920-022-01227-7.

MLA (9th ed.) Citation

Zhou, Jianrong, et al. "Atypical Deletion of Williams–Beuren Syndrome Reveals the Mechanism of Neurodevelopmental Disorders." BMC Medical Genomics, vol. 15, 2022, p. 1, https://doi.org/10.1186/s12920-022-01227-7.