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A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5). [electronic resource] by
- Gardner, Jessica C
- Webb, Tom R
- Kanuga, Naheed
- Robson, Anthony G
- Holder, Graham E
- Stockman, Andrew
- Ripamonti, Caterina
- Ebenezer, Neil D
- Ogun, Olufunmilola
- Devery, Sophie
- Wright, Genevieve A
- Maher, Eamonn R
- Cheetham, Michael E
- Moore, Anthony T
- Michaelides, Michel
- Hardcastle, Alison J
Producer: 20120413
In:
Advances in experimental medicine and biology vol. 723
Availability: No items available.
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5177.
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Visual dysfunction in workers exposed to a mixture of organic solvents. [electronic resource] by
- Gong, Yingyan
- Kishi, Reiko
- Kasai, Setsuko
- Katakura, Yoko
- Fujiwara, Kyoko
- Umemura, Tomohiro
- Kondo, Tomoko
- Sato, Tetsuro
- Sata, Fumihiro
- Tsukishima, Eri
- Tozaki, Shizuka
- Kawai, Toshio
- Miyama, Yuriko
Producer: 20031027
In:
Neurotoxicology vol. 24
Availability: No items available.
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5178.
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Phenotypic characterization of a large family with RP10 autosomal-dominant retinitis pigmentosa: an Asp226Asn mutation in the IMPDH1 gene. [electronic resource] by
- Kozma, Petra
- Hughbanks-Wheaton, Dianna K
- Locke, Kirsten G
- Fish, Garry E
- Gire, Anisa I
- Spellicy, Catherine J
- Sullivan, Lori S
- Bowne, Sara J
- Daiger, Stephen P
- Birch, David G
Producer: 20051222
In:
American journal of ophthalmology vol. 140
Availability: No items available.
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5179.
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