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Ophthalmic Genetics, Volume 22 Issue 4 2001

Ophthalmic Genetics is moving!
ISSN: 1744-5094 (electronic) 1381-6810 (paper)
Publication Frequency: 4 issues per year
Subjects: Genetics; Ophthalmology;
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Non-visual ocular photoreception
Russell N. Van Gelder
Pages 195 – 205
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Neuronal cell death in the visual cortex is a prominent feature of the X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a gene
Lisbeth Tranebjærg;  Peter K. A. Jensen;  Marijke Van Ghelue;  Cindy L. Vnencak-Jones;  Staale Sund;  Kjell Elgjo;  Johannes Jakobsen;  Sigurd Lindal;  Mette Warburg;  Anders Fuglsang-Frederiksen; Kari Skullerud
Pages 207 – 223
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MYOC mutation frequency in primary open-angle glaucoma patients from Western Switzerland
A. Mataftsi;  F. Achache;  E. Héon;  A. Mermoud;  P. Cousin;  G. Metthez;  D. F. Schorderet; F. L. Munier
Pages 225 – 231
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Evaluation of the ELOVL4 gene in patients with age-related macular degeneration
Radha Ayyagari;  Kang Zhang;  Amy Hutchinson;  Zhengya Yu;  Anand Swaroop;  Laura E. Kakuk;  Johanna M. Seddon;  Paul S. Bernstein;  Richard A. Lewis;  Jaana Tammur;  Z. Yang;  Y. Li;  Heidi Zhang;  Beverly M. Yashar;  Jiafan Liu;  Konstantin Petrukhin;  Paul A. Sieving; Rando Allikmets
Pages 233 – 239
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Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1)
John B. Kerrison;  Roberto Giorda;  Thomas D. Lenart;  Arlene V. Drack; Irene H. Maumenee
Pages 241 – 248
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Peripapillary staphyloma associated with orofacial capillary hemangioma
Hayyam Kiratli;  Banu Bozkurt; Cem Mocan
Pages 249 – 253
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