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Genetic Disorders
Citations 71-80 of 188 total displayed.
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Past content
(since May 1998):
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- Correspondence
No Association Between Variations in the WDR36 Gene and Primary Open-Angle Glaucoma
- John H. Fingert; Wallace L. M. Alward; Young H. Kwon; Suma P. Shankar; Jeaneen L. Andorf; David A. Mackey; Val C. Sheffield; Edwin M. Stone
Arch Ophthalmol 2007; 125: 434-a-436-a.
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- Special Articles
Perspective on Genes and Mutations Causing Retinitis Pigmentosa
- Stephen P. Daiger; Sara J. Bowne; Lori S. Sullivan
Arch Ophthalmol 2007; 125: 151-158.
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- Special Articles
Contributions of Genetics to Our Understanding of Inherited Monogenic Retinal Diseases and Age-Related Macular Degeneration
- Dean Bok
Arch Ophthalmol 2007; 125: 160-164.
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- Special Articles
Genetic Origins of Cataract
- Alan Shiels; J. Fielding Hejtmancik
Arch Ophthalmol 2007; 125: 165-173.
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- Special Articles
Genetic Basis of Congenital Strabismus
- Elizabeth C. Engle
Arch Ophthalmol 2007; 125: 189-195.
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- Special Articles
Molecular Diagnosis and Genetic Counseling in Ophthalmology
- Delphine Blain; Brian P. Brooks
Arch Ophthalmol 2007; 125: 196-203.
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- Special Articles
Genetic Testing for Inherited Eye Disease
- Edwin M. Stone
Arch Ophthalmol 2007; 125: 205-212.
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- Ophthalmic Molecular Genetics
New Phenotype Associated With an Arg116Cys Mutation in the CRYAA Gene: Nuclear Cataract, Iris Coloboma, and Microphthalmia
- Francis Beby; Claire Commeaux; Muriel Bozon; Philippe Denis; Patrick Edery; Laurette Morlé
Arch Ophthalmol 2007; 125: 213-216.
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- Ophthalmic Molecular Genetics
Novel USH2A Mutations in Israeli Patients With Retinitis Pigmentosa and Usher Syndrome Type 2
- Nadia Kaiserman; Alexey Obolensky; Eyal Banin; Dror Sharon
Arch Ophthalmol 2007; 125: 219-224.
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- Ophthalmic Molecular Genetics
Retinal Phenotype–Genotype Correlation of Pediatric Patients Expressing Mutations in the Norrie Disease Gene
- Wei-Chi Wu; Kimberly Drenser; Michael Trese; Antonio Capone Jr; Wendy Dailey
Arch Ophthalmol 2007; 125: 225-230.
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