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Ophthalmic Genetics, Volume 24 Issue 3 2003

Ophthalmic Genetics is moving!
ISSN: 1744-5094 (electronic) 1381-6810 (paper)
Publication Frequency: 4 issues per year
Subjects: Genetics; Ophthalmology;
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Ocular manifestations in Fabry disease: a survey of 32 hemizygous male patients
Christophe Orssaud;  Jean Louis Dufier; Dominique Paul Germain
Pages 129 – 139
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Protein expression, genomic structure, and polymorphisms of oculomedin
Nagako Fujiwara;  Toshihiko Matsuo; Hiroshi Ohtsuki
Pages 141 – 151
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Mutational analysis of the MYOCILIN gene in patients with primary open-angle glaucoma in Morocco
Rahma Melki;  Abderrahmane Idhajji;  Said Driouiche;  Moustafa Idrissi Hassani;  Abdelaziz Boukabboucha;  Omar Akhayat;  Henri-Jean Garchon; Ahmed Belmouden
Pages 153 – 160
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PAX6 gene mutations and genotype-phenotype correlations in sporadic cases of aniridia from India
Neeraja Dharmaraj;  Aramati B. M. Reddy;  Velamakanni S. Kiran;  Anil K. Mandal;  Shirly G. Panicker; Subhabrata Chakrabarti
Pages 161 – 165
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Mutational analysis of the OA1 gene in ocular albinism
Olivier Camand;  Sandrine Boutboul;  Laurence Gat;  Laurence Arbogast;  Olivier Roche;  Claude Sternberg;  Joanne Sutherland;  Alex Levin;  Elise Héon;  Maurice Menasche;  Jean-Louis Dufier; Marc Abitbol
Pages 167 – 173
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Interstitial deletion of 13q and a 13;X chromosome translocation results in partial trisomy 13 and bilateral retinoblastoma
David Dries;  Katrina Baca;  Lisa Truss; Sheila Dobin
Pages 175 – 180
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Congenital nasolacrimal duct occlusion with clinical anophthalmos: a possible new association
Halit Oguz;  Adil Ozturk; Imran San
Pages 181 – 185
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One of the genes for Leber congenital amaurosis, AIPL-1, is associated with a cell cycle regulatory protein
Robert K. Koenekoop
Pages 187 – 188
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29th Annual Meeting of EPOS European Paediatric Ophthalmological Society
Page 189
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