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Liu W 13

Showing records 1 to 13 | Display all abstracts from Liu W

82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Wu X
Experimental and therapeutic medicine 2019; 18: 2255-2261
82376 Proteomic analysis of aqueous humor in acute primary angle-closure glaucoma
Wang LM; Dong LJ
Chinese Journal of Ophthalmology 2019; 55: 687-694
82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Xie HN; Wu T
Experimental and therapeutic medicine 2019; 18: 2255-2261
82376 Proteomic analysis of aqueous humor in acute primary angle-closure glaucoma
Liu X
Chinese Journal of Ophthalmology 2019; 55: 687-694
82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Liu W
Experimental and therapeutic medicine 2019; 18: 2255-2261
82376 Proteomic analysis of aqueous humor in acute primary angle-closure glaucoma
Huang LY; Liu W
Chinese Journal of Ophthalmology 2019; 55: 687-694
82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Chen LL
Experimental and therapeutic medicine 2019; 18: 2255-2261
82376 Proteomic analysis of aqueous humor in acute primary angle-closure glaucoma
Lyu YJ
Chinese Journal of Ophthalmology 2019; 55: 687-694
82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Li ZH
Experimental and therapeutic medicine 2019; 18: 2255-2261
82376 Proteomic analysis of aqueous humor in acute primary angle-closure glaucoma
Li XR
Chinese Journal of Ophthalmology 2019; 55: 687-694
82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Wang DJ
Experimental and therapeutic medicine 2019; 18: 2255-2261
82376 Proteomic analysis of aqueous humor in acute primary angle-closure glaucoma
Liu AH
Chinese Journal of Ophthalmology 2019; 55: 687-694
82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Wang Y; Huang HB
Experimental and therapeutic medicine 2019; 18: 2255-2261

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