Ophthalmic Genetics,volume 28,issue 3  (07-2014)

Period of time： 2014年3期

Publisher： Informa Healthcare

Founded in： 1981

Total resources： 61

ISSN： 1381-6810

Subject： R77 Ophthalmology

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Ophthalmic Genetics,volume 28,issue 3

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Leber Congenital Amaurosis: Ciliary Proteins on the Move

By Koenekoop Robert,Cremers Frans,Hollander Anneke I. den in (2007)

Ophthalmic Genetics,volume 28,issue 3 , Vol. 28, Iss. 3, 2007-07 , pp. 111-112

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The Retinal Ciliopathies

By Adams N. A.,Awadein Ahmed,Toma Hassanain in (2007)

Ophthalmic Genetics,volume 28,issue 3 , Vol. 28, Iss. 3, 2007-07 , pp. 113-125

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Rescue of Sight by Gene Therapy - Closer than It May Appear

By Rex Tonia in (2007)

Ophthalmic Genetics,volume 28,issue 3 , Vol. 28, Iss. 3, 2007-07 , pp. 127-133

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Novel Mutations in the KCNV2 Gene in Patients with Cone Dystrophy and a Supernormal Rod Electroretinogram

By Thiagalingam Sureka,McGee Terri,Weleber Richard,Sandberg Michael,Trzupek Karmen,Berson Eliot,Dryja Thaddeus in (2007)

Ophthalmic Genetics,volume 28,issue 3 , Vol. 28, Iss. 3, 2007-07 , pp. 135-142

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Qualitative Research Methodology in the Exploration of Patients' Perceptions of Participating in a Genetic Research Program

By Basson Frieda,Futter Merle Joyce,Greenberg Jacquie in (2007)

Ophthalmic Genetics,volume 28,issue 3 , Vol. 28, Iss. 3, 2007-07 , pp. 143-149

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Screening of the USH1G Gene among Spanish Patients with Usher Syndrome. Lack of Mutations and Evidence of a Minor Role in the Pathogenesis of the Syndrome

By Aller Elena,Jaijo Teresa,Beneyto Magdalena,Nájera Carmen,Morera Constantino,Pérez-Garrigues Herminio,Ayuso Carmen,Millán Jose in (2007)

Ophthalmic Genetics,volume 28,issue 3 , Vol. 28, Iss. 3, 2007-07 , pp. 151-155

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Abnormal Iris Processes May Be a Marker of Glaucoma Gene Carrier Status in Some Cases of Primary Infantile Glaucoma

By Balaratnasingam Chandrakumar,Morgan William,Nelson John,Mackey David,Dimasi David,Lam Geoffrey in (2007)

Ophthalmic Genetics,volume 28,issue 3 , Vol. 28, Iss. 3, 2007-07 , pp. 157-162

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Retinal Dysfunction in Carriers of Bardet-Biedl Syndrome

By Kim Linda,Fishman Gerald,Seiple William,Szlyk Janet,Stone Edwin in (2007)

Ophthalmic Genetics,volume 28,issue 3 , Vol. 28, Iss. 3, 2007-07 , pp. 163-168

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An Unusual Presentation of Macular Corneal Dystrophy Associated with Uniparental Isodisomy and a Novel Leu173Pro Mutation

By Yellore Vivek,Sonmez Baris,Chen Michael,Rayner Sylvia,Thonar Eugene,Aldave Anthony in (2007)

Ophthalmic Genetics,volume 28,issue 3 , Vol. 28, Iss. 3, 2007-07 , pp. 169-174

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Lens Opacities in Bloom Syndrome: Case Report and Review of the Literature

By Cefle Kivanc,Ozturk Sukru,Gozum Nilufer,Duman Nilgun,Mantar Ferhan,Guler Kerim,Palanduz Sukru in (2007)

Ophthalmic Genetics,volume 28,issue 3 , Vol. 28, Iss. 3, 2007-07 , pp. 175-178

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