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Ophthalmic Genetics, Volume 23 Issue 3 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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Vitamin D analogs, a new treatment for retinoblastoma: The first Ellsworth Lecture
Daniel M. Albert;  Robert W. Nickells;  David M. Gamm;  Michele L. Zimbric;  Cassandra L. Schlamp;  Mary J. Lindstrom; Isabelle Audo
Pages 137 – 156
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Electroretinographic findings in Duchenne/Becker muscular dystrophy and correlation with genotype
Ayfer Ülgenalp;  F. Hakan Öner;  Meltem F. Söylev;  Elçin Bora;  Filiz Afrashi;  Süheyla Köse; Derya Erçal
Pages 157 – 165
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Use of denaturing HPLC and automated sequencing to screen the VMD2 gene for mutations associated with Best's vitelliform macular dystrophy
D. Marchant;  K. Gogat;  P. Dureau;  K. Sainton;  C. Sternberg;  S. Gadin;  H. Dollfus;  G. Brasseur;  J. C. Hache;  V. Dumur;  V. Puech;  F. L. Munier;  D. F. Schorderet;  C. Marsac;  M. Menasche;  J. L. Dufier; M. Abitbol
Pages 167 – 174
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Familial unilateral Brown syndrome
Alessandro Iannaccone;  Nathalie McIntosh;  Maria Laura Ciccarelli;  Alfonso Baldi;  P. Alessandro Mutolo;  Salvatore A. Tedesco; Elizabeth C. Engle
Pages 175 – 184
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A case of Moebius syndrome in association with Klinefelter syndrome
Patrick C. Yeh; Michael A. Kipp
Pages 185 – 189
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Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber's hereditary optic neuropathy
Sascha Fauser;  Beate Leo-Kottler;  Dorothea Besch; Janina Luberichs
Pages 191 – 197
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