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✓Human Genetics54
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Li-Lin Lin results 54 · Newest (Page 3/3, per page 25)
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Journal: Human Genetics ×Author: Li-Lin Lin ×Clear All Filters
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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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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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Novel mutations in the IRF6 gene for Van der Woude syndromeNARA Subscribed
Human Genetics · 2003 · Vol. 113 · Issue 5 · Springer
Xiaofang Wang; Jiali Liu; Haibing Zhang; Mingzhen Xiao; Jinfeng Li; Chunling Yang; Xianjun Lin; Zizhong Wu; Landian Hu; Xiangyin Kong
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A common IL-13 Arg130Gln single nucleotide polymorphism among Chinese atopy patients with allergic rhinitisNARA Subscribed
Human Genetics · 2003 · Vol. 113 · Issue 5 · Springer
Min Wang; Zhi-Min Xing; Chao Lu; You-Xiang Ma; De-Lin Yu; Zheng Yan; Shen-Wu Wang; Li-Sheng Yu
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