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Ophthalmic Genetics, Volume 25 Issue 1 2004

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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Announcement
Page 1
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Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador
Stacey M. Curry;  Aline G. Daou;  Pia Hermanns;  Andrea Molinari;  Richard Alan Lewis; Bassem A. Bejjani
Pages 3 – 9
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Genetic analysis of an Indian family with members affected with juvenile-onset primary open-angle glaucoma
M. Markandaya;  T. K. Ramesh;  V. Selvaraju;  Syril K. Dorairaj;  Ravi Prakash;  Jyoti Shetty; A. Kumar
Pages 11 – 23
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Lack of activity of oral etoposide for relapsed intraocular retinoblastoma
Ira J. Dunkel;  Guillermo L. Chantada;  Adriana C. Fandiño; David H. Abramson
Pages 25 – 29
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Fluorine-18 fluorodeoxyglucose positron emission tomography (PET) to detect vital retinoblastoma in the eye: Preliminary experience
A. C. Moll;  O. S. Hoekstra;  S. M. Imhof;  E. F. Comans;  A.Y.N. Schouten-van Meeteren;  P. van der Valk; M. Boers
Pages 31 – 35
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Activity of topotecan in retinoblastoma
Guillermo L. Chantada;  Adriana C. Fandiñ;  Sandra J. Casak;  Gabriel Mato;  Julio Manzitti; Enrique Schvartzman
Pages 37 – 43
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A second primary tumor in a patient with retinoma
Lindy-Anne Korswagen;  Annette C. Moll;  Saskia M. Imhof; Antoinette Y.N. Schouten-van Meeteren
Pages 45 – 48
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Neurofibromatosis type 1 associated with central nervous system lymphoma
Ghassan Zein;  Ellen Yu;  Khaled Tawansy;  András Berta; C. Stephen Foster
Pages 49 – 51
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Ocular manifestations of mosaic trisomy 22: A case report and review of the literature
S. Thomas;  M. Parker;  J. Tan;  D. Duckett; G. Woodruff
Pages 53 – 56
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A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome
Brian P. Brooks;  Sayoko E. Moroi;  Catherine A. Downs;  Shannon Wiltse;  Mohammad I. Othman;  Elena V. Semina; Julia E. Richards
Pages 57 – 62
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Book Review
Richard G. Weleber
Page 63
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Phenotypic variability in three carriers from a family with choroideremia and a frameshift mutation 1388delCCinsG in the REP-1 gene
Günther Rudolph;  Markus Preising;  Petros Kalpadakis;  Christos Haritoglou;  Gabriele E. Lang; Birgit Lorenz
Pages 65 – 66
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