Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: GLB1L3[original query] |
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Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications. Clinical genetics 2022 7 102 (5): 391-403. He Guo-Wei, Maslen Cheryl L, Chen Huan-Xin, Hou Hai-Tao, Bai Xiao-Yan, Wang Xiu-Li, Liu Xiao-Cheng, Lu Wan-Li, Chen Xin-Xin, Chen Wei-Dan, Xing Quan-Sheng, Wu Qin, Wang Jun, Yang Q |
A Genome-Wide Association Study of Prediabetes Status Change. Frontiers in endocrinology 2022 13 881633. Liu Tingting, Li Hongjin, Conley Yvette P, Primack Brian A, Wang Jing, Lo Wen-Juo, Li Changw |
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- Page last updated:Apr 29, 2024
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