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The Journal of Biological Chemistry|July 30, 2020
Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathyYanchun Ji, Juanjuan Zhang, Yuanyuan Lu, et al.Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences|January 5, 2020
[Screening for hereditary tyrosinemia and genotype analysis in newborns]Fan Tong, Rulai Yang, Chang Liu, et al.Frontiers in Cell and Developmental Biology|January 27, 2023
Long-term prognosis of 35 patients with methionine adenosyltransferase deficiency based on newborn screening in ChinaFan Tong, Yuchen Zhang, Chi Chen, et al.Frontiers in Molecular Biosciences|January 3, 2022
Reference Standards for Newborn Screening of Metabolic Disorders by Tandem Mass Spectrometry: A Nationwide Study on Millions of Chinese Neonatal PopulationsFalin He, Rulai Yang, Xinwen Huang, et al.Pageof 5