Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: GDF3[original query] |
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A novel variation of GDF3 in Chinese Han children with a broad phenotypic spectrum of non-syndromic CHDs. Cardiology in the young 2015 Oct 25 (7): 1263-7. Xiao Jianmin, Kang Guanyang, Wang Jing, Li Tengyan, Chen Jiuhao, Wang Jieyin, Li Wei, Wang Binb |
Functional and In Silico Assessment of GDF3 Gene Variants in a Chinese Congenital Scoliosis Population. Medical science monitor : international medical journal of experimental and clinical research 2018 5 24 2992-3001. Chen Jia, Li Xiaoxin, Niu Yuchen, Wu Zhihong, Qiu Guixi |
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome. BMC musculoskeletal disorders 2020 Apr 21 (1): 220. Li Ziquan, Zhao Sen, Cai Siyi, Zhang Yuanqiang, Wang Lianlei, Niu Yuchen, Li Xiaoxin, Hu Jianhua, Chen Jingdan, Wang Shengru, Wang Huizi, Liu Gang, Tian Ye, Wu Zhihong, Zhang Terry Jianguo, , Wang Yipeng, Wu N |
[Clinical Characteristics and Genetic Analysis of Klippel-Feil Syndrome]. Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae 2021 3 43 (1): 25-31. Li Zi Quan, Geng Mo Zhao, Zhao Sen, Wu Zhi Hong, Zhang Jian Guo, Wu Nan, Wang Yi Pe |
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