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Journal of Hazardous Materials|March 10, 2026
Identifying priority pollutants NO2, O3, PM2.5 and PM10 for preventive strategies against birth defects in China: A regional analysisFalin He, Tiancheng Xie, Xinwen Huang, et al.
BMC Medical Ethics|November 26, 2024
Parental awareness and perspectives on newborn screening in China: a questionnaire-based studyXiaoshan Yin, Peiyao Wang, Ziyan Cen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 14, 2020
[Identification of a de novo missense variant of ARID1B gene in a child with mental retardation]Ting Zhang, Qian Wu, Jianbin Yang, et al.
Environmental Pollution (Barking, Essex : 1987)|September 28, 2017
Formation of environmentally relevant polyhalogenated carbazoles from chloroperoxidase-catalyzed halogenation of carbazoleYanqiu Chen, Kunde Lin, Da Chen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 23, 2023
Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency in Zhejiang province, ChinaYi Cheng, Peichun Chen, Zinan Yu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|January 29, 2023
[Analysis of clinical features, biochemical indices and genetic variants among children with Short/branched-chain acyl-CoA dehydrogenase deficiency detected by neonatal screening]HanYi Zhao, Duo Zhou, Haixia Miao, et al.
Molecular Genetics and Metabolism Reports|February 20, 2026
Newborn screening, genetic analysis, and long-term follow-up of 89 cases with short-chain acyl-CoA dehydrogenase deficiency (SCADD)GuLing Qian, Chen Liu, YanHua Xu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 17, 2017
Three novel mutations of ARG1 identified in Chinese patients with argininemia detected by newborn screeningTing Zhang, Jianbin Yang, Xiaoshan Yin, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences|November 19, 2020
[Screening and clinical analysis of isovaleric acidemia newborn in Zhejiang province]Zhenzhen Hu, Jianbin Yang, Lingwei Hu, et al.
European Journal of Medical Genetics|January 19, 2020
A novel SPECC1L mutation causing Teebi hypertelorism syndrome: Expanding phenotypic and genetic spectrumTing Zhang, Qian Wu, Ling Zhu, et al.
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