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Ophthalmic Genetics, Volume 28 Issue 4 2007

Ophthalmic Genetics is moving!
ISSN: 1744-5094 (electronic) 1381-6810 (paper)
Publication Frequency: 4 issues per year
Subjects: Genetics; Ophthalmology;
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Review
A Review of the Molecular Genetics of Congenital Idiopathic Nystagmus (CIN)
James Self; Andrew Lotery
Pages 187 – 191
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Research Article
Pseudo-Vitelliform Macular Detachment and Cuticular Drusen: Exclusion of 6 Candidate Genes
Irene A. Barbazetto;  Nicolas A. Yannuzzi;  Christina M. Klais;  Joanna E. Merriam;  Jana Zernant;  Enrico Peiretti;  Lawrence A. Yannuzzi; Rando Allikmets
Pages 192 – 197
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A New GJA1 (Connexin 43) Mutation Causing Oculodentodigital Dysplasia Associated to Uncommon Features
David Rivera de la Parra; Juan Carlos Zenteno
Pages 198 – 202
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LOC387715/HTRA1 and Complement Factor H Variants in Patients with Age-Related Macular Degeneration Seen at the Mayo Clinic
Jose S. Pulido;  Lisa M. Peterson;  Lejla Mutapcic;  Sandra Bryant; W. Edward Highsmith
Pages 203 – 207
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Case Report
Lens Coloboma Associated with a Ciliary Body Cyst
Arif O. Khan; Abdullah Al-Assiri
Pages 208 – 209
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Chorioretinopathy and Microcephaly with Normal Development
Hoda Ahmadi; Yasmin S. Bradfield
Pages 210 – 215
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Two Novel Deletions (Array CGH Findings) in Pigment Dispersion Syndrome
Ruth Mikelsaar;  Harras Molder;  Oliver Bartsch; Margus Punab
Pages 216 – 219
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Severe Form of Familial Exudative Vitreoretinopathy Caused by Homozygous R417Q Mutation in Frizzled-4 Gene
Hiroyuki Kondo;  Minghui Qin;  Tomoko Tahira;  Eiichi Uchio; Kenshi Hayashi
Pages 220 – 223
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Genetic Screening of Leber Congenital Amaurosis in a Large Consanguineous Iranian Family
Tayebeh Rezaie;  Mohammad-Hassan Karimi-Nejad;  Mohammad-Reza Meshkat;  Saeed Sohbati;  Roxana Karimi-Nejad;  Hossein Najmabadi; Mansoor Sarfarazi
Pages 224 – 228
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Letter To The Editor
Reassessment of the Pathologic Significance of the 9438 Mitochondrial DNA mutation Associated with LHON
Khaled K. Abu-Amero; Thomas M. Bosley
Pages 229 – 230
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Erratum
Erratum
Page 231
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