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Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017.
Liu Z, Yu C, Li Q, Cai R, Qu Y, Wang W, Wang J, Feng J, Zhu W, Ou M, Huang W, Tang D, Guo W, Liu F, Chen Y, Fu L, Zhou Y, Lv W, Zhang H, Zhang J, Wang M, Yang J, Wan K, Miao J, Yuan Z, Liu H, He X, Li W, Chen W, Ye L, Chen Y, Huang S, Liu H, Ding H, Gan X, Wang S, Qiang R, Gong M, Teng P, Wang H, Zhou M, Wei H, Liu X, Tang K, Ma Y, Wu H, Shu X, Chen Y, Zhuang D, Li H, Liu Z, Liu X, Chen Y, Zhu L, Zhu X, Mo C, Tang H, Yin F, Shao Z, Zhang P, Peng B, Lu Q, Wang Z, Zou L. Liu Z, et al. Among authors: ou m. Hum Mutat. 2020 Jan;41(1):212-221. doi: 10.1002/humu.23911. Epub 2019 Sep 23. Hum Mutat. 2020. PMID: 31489982
[Establishment of an auxiliary diagnosis system of newborn screening for inherited metabolic diseases based on artificial intelligence technology and a clinical trial].
Yang RL, Yang YL, Wang T, Xu WZ, Yu G, Yang JB, Sun QL, Gu MS, Li HB, Zhao DH, Pei JY, Jiang T, He J, Zou H, Mao XM, Geng GX, Qiang R, Tian GL, Wang Y, Wei HW, Zhang XG, Wang H, Tian YP, Zou L, Kong YY, Zhou YX, Ou MC, Yao ZR, Zhou YL, Zhu WB, Huang YL, Wang YH, Huang CD, Tan Y, Li L, Shang Q, Zheng H, Lyu SL, Wang WJ, Yao Y, Le J, Shu Q. Yang RL, et al. Among authors: ou mc. Zhonghua Er Ke Za Zhi. 2021 Apr 2;59(4):286-293. doi: 10.3760/cma.j.cn112140-20201209-01089. Zhonghua Er Ke Za Zhi. 2021. PMID: 33775047 Clinical Trial. Chinese.
[Expert consensus on the follow-up of newborn screening for neonatal genetic and metabolic diseases].
Committee For Proficiency Testing Neonatal Genetic Metabolic Disease Screening Center National Health Commission Of China, Ou M, Jiang J, Wang Z. Committee For Proficiency Testing Neonatal Genetic Metabolic Disease Screening Center National Health Commission Of China, et al. Among authors: ou m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Apr 10;37(4):367-372. doi: 10.3760/cma.j.issn.1003-9406.2020.04.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32219815 Chinese.
618 results