Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and PLXNA1[original query] |
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| High-resolution analysis of copy number variants in adults with simple-to-moderate congenital heart disease. American journal of medical genetics. Part A 2013 Dec 161A (12): 3087-94. Zhao Wei, Niu Guannan, Shen Botao, Zheng Yang, Gong Fangchao, Wang Xianfu, Lee Jiyun, Mulvihill John J, Chen Xiaohui, Li Shi |
| Whole-genome and Transcriptome Sequencing of Prostate Cancer Identify New Genetic Alterations Driving Disease Progression. European urology 2017 Sep . Ren Shancheng, Wei Gong-Hong, Liu Dongbing, Wang Liguo, Hou Yong, Zhu Shida, Peng Lihua, Zhang Qin, Cheng Yanbing, Su Hong, Zhou Xiuqing, Zhang Jibin, Li Fuqiang, Zheng Hancheng, Zhao Zhikun, Yin Changjun, He Zengquan, Gao Xin, Zhau Haiyen E, Chu Chia-Yi, Wu Jason Boyang, Collins Colin, Volik Stanislav V, Bell Robert, Huang Jiaoti, Wu Kui, Xu Danfeng, Ye Dingwei, Yu Yongwei, Zhu Lianhui, Qiao Meng, Lee Hang-Mao, Yang Yuehong, Zhu Yasheng, Shi Xiaolei, Chen Rui, Wang Yang, Xu Weidong, Cheng Yanqiong, Xu Chuanliang, Gao Xu, Zhou Tie, Yang Bo, Hou Jianguo, Liu Li, Zhang Zhensheng, Zhu Yao, Qin Chao, Shao Pengfei, Pang Jun, Chung Leland W K, Xu Jianfeng, Wu Chin-Lee, Zhong Weide, Xu Xun, Li Yingrui, Zhang Xiuqing, Wang Jian, Yang Huanming, Wang Jun, Huang Haojie, Sun Yingh |
| Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism. Clinical genetics 2019 Feb 95 (2): 320-324. Kotan Leman D, Isik Emregul, Turan Ihsan, Mengen Eda, Akkus Gamze, Tastan Mehmet, Gurbuz Fatih, Yuksel Bilgin, Topaloglu A Kem |
| Rare variant screening and burden analysis of PLXNA1 in Parkinson's disease. European journal of neurology 2022 7 29 (12): 3737-3741. Li Chunyu, Lin Junyu, Jiang Qirui, Shang Huifa |
- Page last reviewed:Feb 1, 2024
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