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Springer Nature7
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✓Human Genetics7
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Li-hui Lin results 7 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Li-hui Lin ×Clear All Filters
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Novel biallelic LSS variants in autosomal recessive hypotrichosis simplex: insights from a multi-omics approachNARA Subscribed
Human Genetics · 2026 · Vol. 145 · Issue 1 · Springer
Xiaxia Liu; Kai Liu; Yuda Wei; Yongzhen Qi; Yangyang Luo; Tingli Chen; Xiaohua Ye; Junxu Lu; Yunjia Li; Liangqian Jiang; Juan Teng; Xingzhu Geng; Chengcheng Gai; Hongyan Xu; Hui Wang; Lin Li; Chunhai Gao; Xiangyu Zhao
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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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Genome-wide association study identifies HMGN3 locus for spine bone size variation in ChineseNARA Subscribed
Human Genetics · 2012 · Vol. 131 · Issue 3 · Springer
Shu-Feng Lei; Hui Shen; Tie-Lin Yang; Yan Guo; Shan-Shan Dong; Xiang-Hong Xu; Fei-Yan Deng; Qing Tian; Yong-Jun Liu; Yao-Zhong Liu; Jian Li; Hong-Wen Deng
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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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Non-synonymous GIGYF2 variants in Parkinson’s disease from two Asian populationsNARA Subscribed
Human Genetics · 2009 · Vol. 126 · Issue 3 · Springer
Eng-King Tan; Chin-Hslen Lin; Chun-Hwei Tai; Louis C. Tan; Meng-Ling Chen; R. Li; Hui-Qin Lim; Ratnagopal Pavanni; Yih Yuen; K. M. Prakash; Yi Zhao; Ruey-Meei Wu
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A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2–q26.33NARA Subscribed
Human Genetics · 2008 · Vol. 124 · Issue 4 · Springer
Xiao-Hua Dai; Wen-Wu Chen; Xu Wang; Qi-Hui Zhu; Cong Li; Lin Li; Mu-Gen Liu; Qing-K. Wang; Jing-Yu Liu
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A deletion mutation in the ?A1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese familyNARA Subscribed
Human Genetics · 2004 · Vol. 114 · Issue 2 · Springer
Yanhua Qi; Hongyan Jia; Shangzhi Huang; Hui Lin; Jingzhi Gu; Hong Su; Tieying Zhang; Ya Gao; Lijun Qu; Dandan Li; Ying Li
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