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Ophthalmic Genetics, Volume 23 Issue 2 2002

Ophthalmic Genetics is moving!
Official Journal of the International Society for Genetic Eye Disease and Retinoblastoma
ISSN: 1744-5094 (electronic) 1381-6810 (paper)
Publication Frequency: 4 issues per year
Subjects: Genetics; Ophthalmology;
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Infantile and childhood retinal blindness: A molecular perspective (The Franceschetti Lecture)
Richard G. Weleber
Pages 71 – 97
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Electroretinographic changes in the inner retinal layers of the retained eyes of patients with sporadic unilateral retinoblastoma
Wojciech Lubinski;  Stanislaw Zajaczek;  Zbigniew Sych;  Krzysztof Penkala;  Olgierd Palacz; Jan Lubinski
Pages 99 – 107
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Clinical features of achromatopsia in Swedish patients with defined genotypes
Louise Eksandh;  Susanne Kohl; Bernd Wissinger
Pages 109 – 120
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Mutational analysis of the RB1 gene in Indian patients with retinoblastoma
M. Ata-ur-Rasheed;  Geeta K. Vemuganti;  Santosh G. Honavar;  Niyaz Ahmed;  Seyed E. Hasnain; Chitra Kannabiran
Pages 121 – 128
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Identification of a novel VMD2 mutation in Japanese patients with Best disease
Yasuo Yanagi;  Hisaki Sekine; Mikiro Mori
Pages 129 – 133
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An infant with Down syndrome and retinoblastoma. A possible non-fortuitous association
Annette C. Moll;  Saskia M. Imhof;  Lex Bouter;  Willem den Otter; Jan Willem Koten
Pages 135 – 136
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