Age-related macular degeneration-clinical review and genetics update.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 160, doi. 10.1111/cge.12206
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2013 AND VI 84 AND IP 2
Results: 14
1
2
Variations in COL15A1 and COL18A1 influence age of onset of primary open angle glaucoma.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 167, doi. 10.1111/cge.12176
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- Publication type:
- Article
3
Providing comprehensive genetic-based ophthalmic care.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 183, doi. 10.1111/cge.12192
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- Publication type:
- Article
4
Retinal optogenetic therapies: clinical criteria for candidacy.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 175, doi. 10.1111/cge.12165
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- Publication type:
- Article
5
eyeGENE®: a vision community resource facilitating patient care and paving the path for research through molecular diagnostic testing.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 190, doi. 10.1111/cge.12193
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- Publication type:
- Article
6
The golden era of ocular disease gene discovery: Race to the finish.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 99, doi. 10.1111/cge.12204
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- Publication type:
- Article
7
WDR19: An ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior-Loken syndrome.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 150, doi. 10.1111/cge.12196
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- Publication type:
- Article
8
Alternative splicing and retinal degeneration.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 142, doi. 10.1111/cge.12181
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- Publication type:
- Article
9
Genetics of human cataract.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 120, doi. 10.1111/cge.12182
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- Publication type:
- Article
10
Homozygous truncation of SIX6 causes complex microphthalmia in humans.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 198, doi. 10.1111/cge.12046
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- Publication type:
- Article
11
Genes and mutations causing retinitis pigmentosa.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 132, doi. 10.1111/cge.12203
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- Publication type:
- Article
12
Genetics of the corneal endothelial dystrophies: an evidence-based review.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 109, doi. 10.1111/cge.12191
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- Publication type:
- Article
13
Genetic susceptibility and mechanisms for refractive error.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 102, doi. 10.1111/cge.12180
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- Publication type:
- Article
14
Mutations in ALDH1A3 cause microphthalmia.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 2, p. 128, doi. 10.1111/cge.12184
- By:
- Publication type:
- Article