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Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction. [electronic resource] by
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- Thiadens, Alberta A H J
- de Baere, Elfride
- Collin, Rob W J
- Koenekoop, Robert K
- Leroy, Bart P
- van Moll-Ramirez, Norka
- Venselaar, Hanka
- Riemslag, Frans C C
- Cremers, Frans P M
- Klaver, Caroline C W
- den Hollander, Anneke I
Producer: 20130809
In:
Ophthalmology vol. 120
Availability: No items available.
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Pharmacogenetics for genes associated with age-related macular degeneration in the Comparison of AMD Treatments Trials (CATT). [electronic resource] by
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- Sturgill-Short, Gwen M
- Huang, Jiayan
- Callanan, David G
- Kim, Ivana K
- Klein, Michael L
- Maguire, Maureen G
- Martin, Daniel F
Producer: 20130801
In:
Ophthalmology vol. 120
Availability: No items available.
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Inclusion of genotype with fundus phenotype improves accuracy of predicting choroidal neovascularization and geographic atrophy. [electronic resource] by
- Perlee, Lorah T
- Bansal, Aruna T
- Gehrs, Karen
- Heier, Jeffrey S
- Csaky, Karl
- Allikmets, Rando
- Oeth, Paul
- Paladino, Toni
- Farkas, Daniel H
- Rawlings, P Lyle
- Hageman, Gregory S
Producer: 20131119
In:
Ophthalmology vol. 120
Availability: No items available.
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