Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Disease and MSX2[original query] |
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| Single nucleotide polymorphisms of the maternal Msx2 gene and their association with fetal neural tube defects in Han ethnic group in Shanxi Province, China. Chinese medical journal 2011 Feb 124 (3): 374-9. Guo Li, Zhao Hong, Pei Yu-Heng, He Quan-Ren, Li Wan-I, Zhang Ting, Zheng Xiao-Ying, Zhou Ran, Xie J |
| Genome-wide association analysis of common genetic variants of resistant hypertension.
The pharmacogenomics journal 2018 Sep . El Rouby Nihal, McDonough Caitrin W, Gong Yan, McClure Leslie A, Mitchell Braxton D, Horenstein Richard B, Talbert Robert L, Crawford Dana C, , Gitzendanner Matthew A, Takahashi Atsushi, Tanaka Toshihiro, Kubo Michiaki, Pepine Carl J, Cooper-DeHoff Rhonda M, Benavente Oscar R, Shuldiner Alan R, Johnson Julie |
| Dissection of mendelian predisposition and complex genetic architecture of craniovertebral junction malformation. Human genetics 2022 Sep . Liu Zhenlei, Du Huakang, Zhao Hengqiang, Cai Siyi, Zhao Sen, Niu Yuchen, Li Xiaoxin, Liu Bowen, Huang Yingzhao, Shao Jiashen, Liu Lian, Tian Ye, Wu Zhihong, Wu Hao, Hu Yue, Zhang Terry Jianguo, Jian Fengzeng, Wu N |
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