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Ophthalmic Genetics, Volume 23 Issue 4 2002

Ophthalmic Genetics is moving!
ISSN: 1744-5094 (electronic) 1381-6810 (paper)
Publication Frequency: 4 issues per year
Subjects: Genetics; Ophthalmology;
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Evidence of clinical and genetic heterogeneity in autosomal dominant congenital cerulean cataracts
Latifa Hilal;  Emeline Nandrot;  Mohamed Belmekki;  Mohamed Chefchaouni;  Siham El Bacha;  Bouchra Benazzouz;  Yassir Hajaji;  Olivier Gribouval;  Jean-Louis Dufier;  Marc Abitbol; Amina Berraho
Pages 199 – 208
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A pooled case-control study of the apolipoprotein E (APOE) gene in age-related maculopathy
Silke Schmidt;  Caroline C. W. Klaver;  Ann M. Saunders;  Eric A. Postel;  Monica A. De La Paz;  Anita Agarwal;  Kent W. Small;  Nitin Udar;  John M. Ong;  Meenal V. Chalukya;  Anthony Nesburn;  M. Cristina Kenney;  Ruth M. Domurath;  Molly Hogan;  Tammy S. Mah;  Yvette P. Conley;  Robert E. Ferrell;  Daniel E. Weeks;  Paulus T. V. M. de Jong;  Cornelia M. van Duijn;  Jonathan L. Haines;  Margaret A. Pericak-Vance; Michael B. Gorin
Pages 209 – 223
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A novel mutation disrupting the cytoplasmic domain of CRB1 in a large consanguineous family of Palestinian origin affected with Leber congenital amaurosis
Sylvie Gerber;  Isabelle Perrault;  Sylvain Hanein;  Stavit Shalev;  Joel Zlotogora;  Fabienne Barbet;  Dominique Ducroq;  Jean-Louis Dufier;  Arnold Munnich;  Jean-Michel Rozet; Josseline Kaplan
Pages 225 – 235
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TGFBI gene transcript is transforming growth factor-ß1-responsive and cell density-dependent in a human corneal epithelial cell line
Ming X. Wang;  Francis L. Munier;  Kaoru Araki-Saski; Daniel F. Schorderet
Pages 237 – 245
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Corneal decompensation in a boy with Kearns-Sayre syndrome
F. N. Boonstra;  I. Claerhout;  F. A. Hol;  G. P. A. Smit;  J. J. M. van Collenburg; F. M. Meire
Pages 247 – 251
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Fanconi anemia and primary cataracts: first case
M. Merriman;  J. Mora; J. McGaughran
Pages 253 – 255
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Subject Index
Pages 257 – 258
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Author Index
Pages 259 – 260
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Cumulative Table of Contents
Pages 261 – 262
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