GUO Xiangming | Key Laboratory of Ophthalmology of the Ministry of Education and Zhongshan Ophthalmic Center, Sun Ya
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概要
- 同名の論文著者
- Key Laboratory of Ophthalmology of the Ministry of Education and Zhongshan Ophthalmic Center, Sun Yaの論文著者
関連著者
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Jia Xiaoyun
Sun Yat‐sen Univ. Guangzhou Chn
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Guo Xiangming
Sun Yat‐sen Univ. Guangzhou Chn
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GUO Xiangming
Key Laboratory of Ophthalmology of the Ministry of Education and Zhongshan Ophthalmic Center, Sun Ya
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XIAO Xueshan
Key Laboratory of Ophthalmology of the Ministry of Education and Zhongshan Ophthalmic Center, Sun Ya
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LI Shiqiang
Key Laboratory of Ophthalmology of the Ministry of Education and Zhongshan Ophthalmic Center, Sun Ya
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JIA Xiaoyun
Key Laboratory of Ophthalmology of the Ministry of Education and Zhongshan Ophthalmic Center, Sun Ya
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ZHANG Qingjiong
Key Laboratory of Ophthalmology of the Ministry of Education and Zhongshan Ophthalmic Center, Sun Ya
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SHEN Huangxuan
Key Laboratory of Ophthalmology of the Ministry of Education and Zhongshan Ophthalmic Center, Sun Ya
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DAI Qilin
Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University
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HEJTMANCIK J.
Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Healt
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YANG Zhikuan
Key Laboratory of Ophthalmology of the Ministry of Education and Zhongshan Ophthalmic Center, Sun Ya
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WANG Panfeng
Key Laboratory of Ophthalmology of the Ministry of Education, Sun Yat-sen University
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Wang Panfeng
Key Laboratory Of Ophthalmology Of The Ministry Of Education Sun Yat-sen University
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Hejtmancik J.
Ophthalmic Genetics And Visual Function Branch National Eye Institute National Institutes Of Health
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Shen Huangxuan
Key Laboratory Of Ophthalmology Of The Ministry Of Education And Zhongshan Ophthalmic Center Sun Yat
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Yang Zhikuan
Key Laboratory Of Ophthalmology Of The Ministry Of Education And Zhongshan Ophthalmic Center Sun Yat
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Dai Qilin
Department Of Neurology The First Affiliated Hospital Sun Yat-sen University
著作論文
- Cataracts, ataxia, short stature, and mental retardation in a Chinese family mapped to Xpter-q13.1
- CSNB1 in Chinese families associated with novel mutations in NYX
- Linkage analysis of two families with X-linked recessive congenital motor nystagmus