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The British Journal of Ophthalmology|December 24, 2004
Acute zonal occult outer retinopathy: towards a set of diagnostic criteriaP J Francis, A Marinescu, F W Fitzke, et al.
Journal of Medical Genetics|February 1, 1994
Partial trisomy 3q causing mild Cornelia de Lange phenotypeS E Holder, L M Grimsley, R W Palmer, et al.
Journal of Medical Genetics|September 1, 1993
Exclusion of candidate genes from a role in cleft lip with or without cleft palate: linkage and association studiesG M Vintiner, K K Lo, S E Holder, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|November 12, 2013
The importance of electrophysiology in revealing a complete homozygous deletion of KCNV2John R Grigg, Graham E Holder, Francis A Billson, et al.
The British Journal of Ophthalmology|July 20, 2004
Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritanceS A Kabanarou, G E Holder, F W Fitzke, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 11, 2002
Clinical variations in assessment of bull's-eye maculopathyMalaika M Kurz-Levin, Anthony S Halfyard, Catey Bunce, et al.
Ophthalmic Surgery, Lasers & Imaging Retina|April 19, 2017
Unilateral Pigmented Paravenous Retinochoroidal Atrophy Associated With Presumed Ocular TuberculosisGuillermo Fernandez-Sanz, Ester Carreño, Sonia Mall, et al.
The British Journal of Ophthalmology|May 29, 2003
The clinical features of albinism and their correlation with visual evoked potentialsS E Dorey, M M Neveu, L C Burton, et al.
Clinical Dysmorphology|July 19, 2003
Septo-optic dysplasia, subglottic stenosis and skeletal abnormalities: a case reportEmma L Wakeling, Mehul T Dattani, A Bloch-Zupan, et al.
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