The homeobox gene Otx2 in development and disease von Beby, Francis, Lamonerie, Thomas

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Loss of Otx2 in the adult retina disrupts retinal pigment epithelium function, causing photoreceptor degeneration von Housset, Michael, Samuel, Alexander, Ettaiche, Mohamed, Bemelmans, Alexis, Béby, Francis, Billon, Nathalie, Lamonerie, Thomas

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Otx2 gene deletion in adult mouse retina induces rapid RPE dystrophy and slow photoreceptor degeneration von Béby, Francis, Housset, Michael, Fossat, Nicolas, Le Greneur, Coralie, Flamant, Frédéric, Godement, Pierre, Lamonerie, Thomas

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Nonpenetrating External Trabeculectomy for Congenital Glaucoma von Roche, Olivier, MD, Beby, Francis, MD, Parsa, Afshin, MD, MPH, Orssaud, Christophe, MD, Dufier, Jean-Louis, MD, Parsa, Cameron F., MD

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A new GFP-tagged line reveals unexpected Otx2 protein localization in retinal photoreceptors von Fossat, Nicolas, Le Greneur, Coralie, Béby, Francis, Vincent, Stéphane, Godement, Pierre, Chatelain, Gilles, Lamonerie, Thomas

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A [c.566-2A>G] heterozygous mutation in the PAX6 gene causes aniridia with mild visual impairment von Beby, F, Dieterich, K, Calvas, P

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Nonpenetrating external trabeculectomy for congenital glaucoma : A retrospective study von ROCHE, Olivier, BEBY, Francis, PARSA, Afshin, ORSSAUD, Christophe, DUFIER, Jean-Louis, PARSA, Cameron F

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Coats' disease and bilateral cataract in a child with Turner syndrome: a case report von Beby, F, Roche, O, Burillon, C, Denis, P

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Anterior segment dysgenesis in a child with factor VII deficiency von Beby, Francis, Meunier, Sandrine, Cochat, Pierre, Roche, Olivier, Aptel, Florent, Burillon, Carole, Denis, Philippe

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Ocular Anomalies Associated with Interstitial Deletion of Chromosome 2q31: Case Report and Review von Gambrelle, Joël, Till, Marianne, Lukusa, Bibi, Beby, Francis, Mory, Nathalie, Sann, Léon, Kodjikian, Laurent, Grange, Jean Daniel, Putet, Guy

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New Phenotype Associated With an Arg116Cys Mutation in the CRYAA Gene: Nuclear Cataract, Iris Coloboma, and Microphthalmia von Beby, Francis, Commeaux, Claire, Bozon, Muriel, Denis, Philippe, Edery, Patrick, Morlé, Laurette

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New Phenotype Associated With an Arg 116 Cys Mutation in the CRYAA Gene von Beby, Francis, Commeaux, Claire, Bozon, Muriel, Denis, Philippe

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Descemet Membrane Rupture Accompanied by Stromal Clefting in Congenital Glaucoma von Roche, Olivier, Beby, Francis, Dufier, Jean-Louis, Parsa, Cameron F

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New phenotype associated with an argll6cys mutation in the CRYAA gene : Nuclear cataract, iris coloboma, and microphthalmia von BEBY, Francis, COMMEAUX, Claire, BOZON, Muriel, DENIS, Philippe, EDERY, Patrick, MORLE, Laurette

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Penetrating ocular injuries in children: visual outcome and prognostic factors von Beby, Francis, Roche, Olivier, Kodjikian, Laurent, Abbas, Fatima, Kouassi, Noelle, Burillon, Carole, Denis, Philippe

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Anterior segment dysgenesis in a child with factor VII deficiency von Beby, Francis, Meunier, Sandrine, Cochat, Pierre, Roche, Olivier, Aptel, Florent, Burillon, Carole, Denis, Philippe

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The structure of targeting vector (first line), wild type locus (second line), targeted allele after homologous recombination (third line) and allele after removal of the cassette... von Fossat, Nicolas, Greneur, Coralie Le, Béby, Francis, Vincent, Stéphane, Godement, Pierre, Chatelain, Gilles, Lamonerie, Thomas

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A new GFP-tagged line reveals unexpected Otx2 protein localization in retinal photoreceptors-1 von Fossat, Nicolas, Greneur, Coralie Le, Béby, Francis, Vincent, Stéphane, Godement, Pierre, Chatelain, Gilles, Lamonerie, Thomas

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GFP fluorescence and transmission observations of and control embryos at E6 von Fossat, Nicolas, Greneur, Coralie Le, Béby, Francis, Vincent, Stéphane, Godement, Pierre, Chatelain, Gilles, Lamonerie, Thomas

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Direct visualisation of GFP fluorescence (green) and propidium iodide staining of DNA (red) on 10 μm thin section of () and control () adult retina von Fossat, Nicolas, Greneur, Coralie Le, Béby, Francis, Vincent, Stéphane, Godement, Pierre, Chatelain, Gilles, Lamonerie, Thomas

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