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Ophthalmic Genetics, Volume 26 Issue 3 2005

Ophthalmic Genetics is moving!
ISSN: 1744-5094 (electronic) 1381-6810 (paper)
Publication Frequency: 4 issues per year
Subjects: Genetics; Ophthalmology;
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Research Report
Juvenile X-Linked Retinoschisis with Normal Scotopic b-Wave in the Electroretinogram at an Early Stage of the Disease
Louise Eksandh;  Sten Andréasson; Magnus Abrahamson
Pages 111 – 117
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Clinical Phenotype in a Swedish Family with a Mutation in the IMPDH1 Gene
Patrik Schatz;  Vesna Ponjavic;  Sten Andréasson;  Terri L. McGee;  Thaddeus P. Dryja; Magnus Abrahamson
Pages 119 – 124
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Posterior Polar Cataract: Genetic Analysis of a Large Family
Simone Finzi;  Yingying Li;  Thomas N. Mitchell;  Arman Farr;  Irene H. Maumenee;  Juliana M. F. Sallum; Olof Sundin
Pages 125 – 130
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Case Report
A New Case of Oculoectodermal Syndrome
Thomas K. M. Lee;  Royce L. C. Johnson;  Ian M. MacDonald;  Alfons L. Krol; J. Stephen Bamforth
Pages 131 – 133
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Rieger's Anomaly and Other Ocular Abnormalities in Association with Osteogenesis Imperfecta and a COL1A1 Mutation
Benjamin U. Nwosu *;  Margarita Raygada;  Ekaterini T. Tsilou;  Owen M. Rennert; Constantine A. Stratakis
Pages 135 – 138
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Mild Optic Nerve Hypoplasia with Retinal Venous Tortuosity in Aarskog (Facial-Digital-Genital) Syndrome
Aryan Jogiya; Charles Sandy
Pages 139 – 141
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Ophthalmic Aspects of GAPO Syndrome: Case Report and Review
Priscila Hae Hyun Rim; Antonia Paula Marques-de-Faria
Pages 143 – 147
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Abstract
The Sun King, Leber Hereditary Optic Neuropathy, and Quebec: An Example of the Founder Effect
Robert K. Koenekoop
Page 149
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Letter To The Editor
Association Down Syndrome-Retinoblatoma: A New Observation
Daniel Satgè;  Daniel F. Schorderet;  Aubin Balmer;  Maja Beck-Popovic;  Marie Claude Addor;  Jacques S. Beckmann; Francis L. Munier
Pages 151 – 152
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