APA (7th ed.) Citation

Zhao, J., Lyu, G., Ding, C., Wang, X., Li, J., Zhang, W., . . . Zhang, V. W. (2022). Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patients. Molecular Genetics & Genomic Medicine, 10(3), 1. https://doi.org/10.1002/mgg3.1825

Chicago Style (17th ed.) Citation

Zhao, Jianbo, Guizhen Lyu, Changhong Ding, Xiaohui Wang, Jiuwei Li, Weihua Zhang, Xinying Yang, and Victor Wei Zhang. "Expanding the Mutational Spectrum of Rahman Syndrome: A Rare Disorder with Severe Intellectual Disability and Particular Facial Features in Two Chinese Patients." Molecular Genetics & Genomic Medicine 10, no. 3 (2022): 1. https://doi.org/10.1002/mgg3.1825.

MLA (9th ed.) Citation

Zhao, Jianbo, et al. "Expanding the Mutational Spectrum of Rahman Syndrome: A Rare Disorder with Severe Intellectual Disability and Particular Facial Features in Two Chinese Patients." Molecular Genetics & Genomic Medicine, vol. 10, no. 3, 2022, p. 1, https://doi.org/10.1002/mgg3.1825.