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Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism.
Schaaf CP, Gonzalez-Garay ML, Xia F, Potocki L, Gripp KW, Zhang B, Peters BA, McElwain MA, Drmanac R, Beaudet AL, Caskey CT, Yang Y. Schaaf CP, et al. Among authors: zhang b. Nat Genet. 2013 Nov;45(11):1405-8. doi: 10.1038/ng.2776. Epub 2013 Sep 29. Nat Genet. 2013. PMID: 24076603 Free PMC article.
Dietary Vitamin Intake Among Chinese Adults - 10 PLADs, China, 2022-2023.
Zhang X, Su C, Zhang J, Huang F, Du W, Jia X, Ouyang Y, Li L, Bai J, Wei Y, Guan F, He Y, Zhang B, Wang H. Zhang X, et al. Among authors: zhang b. China CDC Wkly. 2024 Dec 20;6(51):1365-1369. doi: 10.46234/ccdcw2024.271. China CDC Wkly. 2024. PMID: 39802084 Free PMC article.
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