Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China.

MLA

Yang-Li, Dai, et al. “Recommendations for the Diagnosis and Management of Childhood Prader-Willi Syndrome in China.” Orphanet Journal of Rare Diseases, vol. 17, no. 1, June 2022, pp. 1–13. EBSCOhost, https://doi.org/10.1186/s13023-022-02302-z.

APA

Yang-Li, D., Fei-Hong, L., Hui-Wen, Z., Ming-Sheng, M., Xiao-Ping, L., Li, L., Yi, W., Qing, Z., Yong-Hui, J., Chao-Chun, Z., PWS Cooperation Group of Rare Diseases Branch of Chinese Pediatric Society, Xiao-Ou, S., Yu, Y., Hui-Feng, Z., Zhi-Liang, T., Bo, S., Mei, L., Ya-Ying, C., Ying, Y., & Xiong-Ying, Y. (2022). Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China. Orphanet Journal of Rare Diseases, 17(1), 1–13. https://doi.org/10.1186/s13023-022-02302-z

Chicago

Yang-Li, Dai, Luo Fei-Hong, Zhang Hui-Wen, Ma Ming-Sheng, Luo Xiao-Ping, Liu Li, Wang Yi, et al. 2022. “Recommendations for the Diagnosis and Management of Childhood Prader-Willi Syndrome in China.” Orphanet Journal of Rare Diseases 17 (1): 1–13. doi:10.1186/s13023-022-02302-z.