APA (7th ed.) Citation

Zhao, S., Zhang, Y., Hallgrimsdottir, S., Zuo, Y., Li, X., Batkovskyte, D., . . . Wu, N. (2022). Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders. Npj genomic medicine, 7(1), 11. https://doi.org/10.1038/s41525-021-00273-x

Chicago Style (17th ed.) Citation

Zhao, Sen, et al. "Expanding the Mutation and Phenotype Spectrum of MYH3-associated Skeletal Disorders." Npj Genomic Medicine 7, no. 1 (2022): 11. https://doi.org/10.1038/s41525-021-00273-x.

MLA (9th ed.) Citation

Zhao, Sen, et al. "Expanding the Mutation and Phenotype Spectrum of MYH3-associated Skeletal Disorders." Npj Genomic Medicine, vol. 7, no. 1, 2022, p. 11, https://doi.org/10.1038/s41525-021-00273-x.