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Ophthalmic Genetics|April 26, 2000
Morning glory disk anomaly, choroidal coloboma, and congenital constrictive malformations of the internal carotid arteries (moyamoya disease)C Krishnan, A Roy, E TraboulsiOphthalmic Genetics|August 1, 2000
Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 geneL B Eksandh, V B Ponjavic, P B Munroe, et al.Ophthalmic Genetics|August 1, 2000
Apple peel atresia in association with bilateral colobomatous malformation of the optic nerve heads, dysmorphic features, and learning disability - a new syndrome?F M Waters, I C Lloyd, J Clayton-SmithOphthalmic Genetics|July 27, 1999
Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt diseaseM F Kniazeva, M F Chiang, G R Cutting, et al.Ophthalmic Genetics|July 27, 1999
No missense mutation in choroideremia patients analyzed to dateL Beaufrère, M Claustres, S TufferyOphthalmic Genetics|July 27, 1999
Visual impairment and REP-1 gene mutations in Japanese choroideremia patientsM Hayakawa, K Fujiki, Y Hotta, et al.Ophthalmic Genetics|October 18, 2000
Optic atrophy in association with cobalamin C (cblC) diseaseN Patton, S Beatty, I C Lloyd, et al.Ophthalmic Genetics|March 23, 2001
Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomaliesL Lavanchy, F L Munier, P Cousin, et al.Ophthalmic Genetics|July 13, 2001
Association of retinopathy with a microsatellite at 5' end of the aldose reductase gene in Chinese patients with late-onset Type 2 diabetesS C Lee, Y Wang, G T Ko, et al.Ophthalmic Genetics|July 13, 2001
Osteosarcoma following retinoblastoma: age at onset and latency periodL Chauveinc, V Mosseri, E Quintana, et al.Pageof 185