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Springer Nature3
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✓Human Genetics3
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Li-Mei Sun results 3 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Li-Mei Sun ×Clear All Filters
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ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing lossNARA Subscribed
Human Genetics · 2018 · Vol. 137 · Issue 4 · Springer
Wu Li; Jie Sun; Jie Ling; Jiada Li; Chufeng He; Yalan Liu; Hongsheng Chen; Meichao Men; Zhijie Niu; Yuyuan Deng; Meng Li; Taoxi Li; Jie Wen; Shushan Sang; Haibo Li; Zhengqing Wan; Elodie M. Richard; Prem Chapagain; Denise Yan; Xue Zhong Liu; Lingyun Mei; Yong Feng
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Polymorphisms of the Interleukin 6 gene contribute to cervical cancer susceptibility in Eastern Chinese womenNARA Subscribed
Human Genetics · 2013 · Vol. 132 · Issue 3 · Springer
Ting-Yan Shi; Mei-Ling Zhu; Jing He; Meng-Yun Wang; Qiao-Xin Li; Xiao-Yan Zhou; Meng-Hong Sun; Zhi-Ming Shao; Ke-Da Yu; Xi Cheng; Xiaohua Wu; Qingyi Wei
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Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type IINARA Subscribed
Human Genetics · 2012 · Vol. 131 · Issue 3 · Springer
Hua Zhang; Hongsheng Chen; Hunjin Luo; Jing An; Lin Sun; Lingyun Mei; Chufeng He; Lu Jiang; Wen Jiang; Kun Xia; Jia-Da Li; Yong Feng
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