Jinying Wu, Meifang Lei, Xuetao Wang, Nan Liu, Xiaowei Xu, Chunyu Gu, . . . Wei Liu. (2022). Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: A case report. BMC.
Chicago Style (17th ed.) CitationJinying Wu, Meifang Lei, Xuetao Wang, Nan Liu, Xiaowei Xu, Chunyu Gu, Yuping Yu, and Wei Liu. Prader-Willi Syndrome Patient with Atypical Phenotypes Caused by Mosaic Deletion in the Paternal 15q11-q13 Region: A Case Report. BMC, 2022.
MLA (9th ed.) CitationJinying Wu, et al. Prader-Willi Syndrome Patient with Atypical Phenotypes Caused by Mosaic Deletion in the Paternal 15q11-q13 Region: A Case Report. BMC, 2022.
Warning: These citations may not always be 100% accurate.