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Springer Nature8
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✓Human Genetics8
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Li-Mei Lin results 8 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Li-Mei Lin ×Clear All Filters
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Identification of genetic associations of SP110/MYBBP1A/RELA with pulmonary tuberculosis in the Chinese Han populationNARA Subscribed
Human Genetics · 2013 · Vol. 132 · Issue 3 · Springer
Lei Cai; Shao-Li Deng; Li Liang; Hui Pan; Jia Zhou; Mei-Yan Wang; Jun Yue; Chun-Ling Wan; Guang He; Lin He
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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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The CAG repeat in SCA12 functions as a cis element to up-regulate PPP2R2B expressionNARA Subscribed
Human Genetics · 2010 · Vol. 128 · Issue 2 · Springer
Chih-Hsin Lin; Chiung-Mei Chen; Yi-Ting Hou; Yih-Ru Wu; Hsiu-Mei Hsieh-Li; Ming-Tsan Su; Guey-Jen Lee-Chen
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Erratum to: Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing lossNARA Subscribed
Human Genetics · 2010 · Vol. 127 · Issue 5 · Springer
Hui-Mei Hong; Jiann-Jou Yang; Jia-Ching Shieh; Mei-Ling Lin; Shuan-Yow Li
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Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31NARA Subscribed
Human Genetics · 2009 · Vol. 125 · Issue 1 · Springer
Xue-Zhong Liu; Yongyi Yuan; Denise Yan; Emilie Hong Ding; Xiao Mei Ouyang; Yu Fei; Wenxue Tang; Huijun Yuan; Qing Chang; Li Lin Du; Xin Zhang; Guojian Wang; Shoeb Ahmad; Dong Yang Kang; Xi Lin; Pu Dai
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Genome-wide association scan for stature in Chinese: evidence for ethnic specific lociNARA Subscribed
Human Genetics · 2009 · Vol. 125 · Issue 1 · Springer
Shu-Feng Lei; Tie-Lin Yang; Li-Jun Tan; Xiang-Ding Chen; Yan Guo; Yan-Fang Guo; Liang Zhang; Xiao-Gang Liu; Han Yan; Feng Pan; Zhi-Xin Zhang; Yu-Mei Peng; Qi Zhou; Li-Na He; Xue-Zhen Zhu; Jing Cheng; Yao-Zhong Liu; Christopher J. Papasian; Hong-Wen Deng
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Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationNARA Subscribed
Human Genetics · 2005 · Vol. 116 · Issue 4 · Springer
Xiao Mei Ouyang; Denise Yan; Li Lin Du; J. Fielding. Hejtmancik; Samuel G. Jacobson; Walter E. Nance; An Ren Li; Simon Angeli; Muriel Kaiser; Valerie Newton; Steve D. M. Brown; Thomas Balkany; Xue Zhong Liu
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Evidence of a founder effect for the 235delC mutation of GJB2 (connexin�26) in east AsiansNARA Subscribed
Human Genetics · 2003 · Vol. 114 · Issue 1 · Springer
Denise Yan; Hong-Joon Park; Xiao Mei Ouyang; Arti Pandya; Katsumi Doi; Raadnabazar Erdenetungalag; Li Lin Du; Naoki Matsushiro; Walter E. Nance; Andrew J. Griffith; Xue Zhong Liu
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