Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: ARHGEF18[original query] |
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Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease). Rare diseases (Austin, Tex.) 2013 Dec 1 (1): 1. Xie Zhihui, Nagarajan Vijayaraj, Sturdevant Daniel E, Iwaki Shoko, Chan Eunice, Wisch Laura, Young Michael, Nelson Celeste M, Porcella Stephen F, Druey Kirk |
Association between a Single Nucleotide Polymorphism in the 3'-UTR of ARHGEF18 and the Risk of Nonidiopathic Pulmonary Arterial Hypertension in Chinese Population. Disease markers 2018 11 2018 2461845. Li Ding, Sun Yan, Kong Xiaochao, Luan Changxing, Yu Youjia, Chen Feng, Chen Pe |
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- Page last updated:Apr 22, 2024
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