[1] |
Wei Zhenyu, Xu Ke, Liang Qingfeng.
Clinical characteristics under in vivo confocal microscopy and TGFBI gene mutation analysis in Thiel-Behnke corneal dystrophy
[J]. Ophthalmology in China, 2020, 29(3): 173-179.
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[2] |
Yan Bojing1, Lang Xuqiang1, Sun Xiaowei2, Yang Liping3, Li Genlin4.
Novel mutations of RPGR in Chinese families with X-linked retinitis pigmentosa
[J]. Ophthalmology in China, 2020, 29(3): 180-186.
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[3] |
Li Yang.
Opportunities and challenges of clinical and basic research on Bietti crystalline dystrophy
[J]. Ophthalmology in China, 2020, 29(2): 84-86.
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[4] |
Xu Ke, Zhang Xiaohui, Xie Yue, Ye Hanwen, You Bing, Li Yang.
Clinical features of Bietti crystalline corneoretinal dystrophy caused by mutations in the CYP4V2 gene
[J]. Ophthalmology in China, 2020, 29(2): 93-97.
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[5] |
CHEN Chun-jie, XIAO Ting, XU Ke, XIE Yue, ZHANG Xiao-hui, LI Yang.
Genetic and phenotype characteristics analysis of two Waardenburg syndrome families
[J]. Ophthalmology in China, 2019, 28(3): 212-218.
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[6] |
LI Bei-han1, SONG Xu-dong2.
Surgical treatment and pedigree analysis of FBN1 mutation for a Chinese family with isolated ectopia lentis
[J]. Ophthalmology in China, 2018, 27(2): 85-90.
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[7] |
GUO Zheng1, LI Shi-lian1, XIANG Dao-man2.
The characteristics and management of posterior capsule in congenital cataract
[J]. Ophthalmology in China, 2018, 27(2): 91-94.
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[8] |
WEI Ai-hua1, ZHANG Ying-zi1, BAI Da-yong2, LIU Teng1, YANG Xiu-min1.
Analysis of GPR143 gene in Chinese Han patients with ocular albinism type 1
[J]. Ophthalmology in China, 2017, 26(4): 224-229.
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[9] |
GONG Li-xue, GU Hong, LIU Shou-bin, LIU Ning-pu, MA Kai.
Two novel mutations in Best vitelliform macular dystrophy GONG
[J]. Ophthalmology in China, 2017, 26(3): 195-199.
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[10] |
LI Yang.
Molecuar genetic analysis in the diagnosis for sporadic patients with optic neuropathies
[J]. Ophthalmology in China, 2015, 24(2): 73-75.
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[11] |
XIE Yue, CHEN Jie-qiong, XU Ke, LIU Li-juan, ZHANG Xiao-hui, JIANG Feng, DONG Bing, LI Yang.
Characteristics of OPA1 genotype in Chinese patients with suspected hereditary optic atrophy
[J]. Ophthalmology in China, 2015, 24(2): 79-84.
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[12] |
XIE Yue, CHEN Jie-qiong, XU Ke, LIU Li-juan, ZHANG Xiao-hui, JIANG Feng, DONG Bing, LI Yang.
Mitochondria DNA mutation detection and clinical features in Chinese patients with suspected hereditary optic atrophy
[J]. Ophthalmology in China, 2015, 24(2): 85-89.
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[13] |
JIANG Feng, CHEN Jie-qiong, XU Ke, ZHANG Xiao-hui, LI Yang.
Characteristics of RS1 genotype in Chinese patients with X-linked retinoschisis
[J]. Ophthalmology in China, 2015, 24(2): 90-95.
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[14] |
MA Yan, LU Hai.
Etiology and clinical characteristics of infantile cataract combined with vitreous abnormities
[J]. Ophthalmology in China, 2015, 24(2): 103-107.
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[15] |
ZHOU Min1, WANG Chun-fang1, LIANG Qing-feng2.
Study of βIGH3 gene mutation in a Chinese pedigree with Avellino corneal dystrophy
[J]. Ophthalmology in China, 2014, 23(3): 152-156.
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