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October 2016 - January 1929

Decade

Year

Issue

February 1, 2007, Vol 125, No. 2, Pages 150-280 | Ophthalmic Genetics

Special Article

Perspective on Genes and Mutations Causing Retinitis Pigmentosa

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Arch Ophthalmol. 2007;125(2):151-158. doi:10.1001/archopht.125.2.151

Contributions of Genetics to Our Understanding of Inherited Monogenic Retinal Diseases and Age-Related Macular Degeneration

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Arch Ophthalmol. 2007;125(2):160-164. doi:10.1001/archopht.125.2.160

Genetic Origins of Cataract

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Arch Ophthalmol. 2007;125(2):165-173. doi:10.1001/archopht.125.2.165

Elucidating the Molecular Genetic Basis of the Corneal DystrophiesAre We There Yet?

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Arch Ophthalmol. 2007;125(2):177-186. doi:10.1001/archopht.125.2.177

Genetic Basis of Congenital Strabismus

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Arch Ophthalmol. 2007;125(2):189-195. doi:10.1001/archopht.125.2.189

Molecular Diagnosis and Genetic Counseling in Ophthalmology

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Arch Ophthalmol. 2007;125(2):196-203. doi:10.1001/archopht.125.2.196

Genetic Testing for Inherited Eye Disease

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Arch Ophthalmol. 2007;125(2):205-212. doi:10.1001/archopht.125.2.205
Archives Web Quiz Winner

September 2006 Archives Web Quiz Winner

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Arch Ophthalmol. 2007;125(2):212-212. doi:10.1001/archopht.125.2.212
Ophthalmic Molecular Genetics

New Phenotype Associated With an Arg116Cys Mutation in the CRYAA GeneNuclear Cataract, Iris Coloboma, and Microphthalmia

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Arch Ophthalmol. 2007;125(2):213-216. doi:10.1001/archopht.125.2.213
Call for Papers

Poverty and Human Development and Ophthalmology

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Arch Ophthalmol. 2007;125(2):216-216. doi:10.1001/archopht.125.2.216

Novel USH2A Mutations in Israeli Patients With Retinitis Pigmentosa and Usher Syndrome Type 2

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Arch Ophthalmol. 2007;125(2):219-224. doi:10.1001/archopht.125.2.219

Retinal Phenotype–Genotype Correlation of Pediatric Patients Expressing Mutations in the Norrie Disease Gene

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Arch Ophthalmol. 2007;125(2):225-230. doi:10.1001/archopht.125.2.225

Medical Education and Ophthalmology

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Arch Ophthalmol. 2007;125(2):230-230. doi:10.1001/archopht.125.2.230

Retinopathy in Danon Disease

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Arch Ophthalmol. 2007;125(2):231-236. doi:10.1001/archopht.125.2.231

Genotype-Phenotype Correlation in von Hippel-Lindau Disease With Retinal Angiomatosis

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Arch Ophthalmol. 2007;125(2):239-245. doi:10.1001/archopht.125.2.239

Nitric Oxide Synthase and Superoxide Dismutase Gene Polymorphisms in Behçet Disease

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Arch Ophthalmol. 2007;125(2):246-251. doi:10.1001/archopht.125.2.246
Clinical Sciences

Molecular Testing for Hereditary Retinal Disease as Part of Clinical Care

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Arch Ophthalmol. 2007;125(2):252-258. doi:10.1001/archopht.125.2.252

Violence/Human Rights and Ophthalmology

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Arch Ophthalmol. 2007;125(2):258-258. doi:10.1001/archopht.125.2.258

Novel Phenotypic and Genotypic Findings in X-Linked Retinoschisis

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Arch Ophthalmol. 2007;125(2):259-267. doi:10.1001/archopht.125.2.259
Laboratory Sciences

Use of Mitochondrial Antioxidant Defenses for Rescue of Cells With a Leber Hereditary Optic Neuropathy–Causing Mutation

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Arch Ophthalmol. 2007;125(2):268-272. doi:10.1001/archopht.125.2.268
Clinicopathologic Reports, Case Reports, and Small Case Series

Catastrophic Visual Loss in a Patient With Friedreich Ataxia

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Arch Ophthalmol. 2007;125(2):273-274. doi:10.1001/archopht.125.2.273

Autofluorescence Findings in Acute Exudative Polymorphous Vitelliform Maculopathy

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Arch Ophthalmol. 2007;125(2):274-277. doi:10.1001/archopht.125.2.274
Photo Essay

Outer Retinal Corrugations in X-Linked Juvenile Retinoschisis

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Arch Ophthalmol. 2007;125(2):278-279. doi:10.1001/archopht.125.2.278

Classic Features of Multiple Endocrine Neoplasia Type 2B

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Arch Ophthalmol. 2007;125(2):280-280. doi:10.1001/archopht.125.2.280
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