Mutations in RPE65 cause Leber's congenital amaurosis von Harris, Eddie, Claustres, Mireille, Liu, Su-Yan, Zrenner, Eberhart, Amalric, Pierre, Hamel, Christian P, Griffoin, Jean-Michel, Bareil, Corinne, Redmond, T. Michael, Marlhens, Françoise, Arnaud, Bernard, Eliaou, Claudie

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Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene von Marlhens, Françoise, Griffoin, Jean-Michel, Bareil, Corinne, Arnaud, Bernard, Claustres, Mireille, Hamel, Christian P

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X-linked retinoschisis with a novel substitutive amino acid (P193S) in XLRS1 von Duval, Pierre-André, Marlhens, Françoise, Griffoin, Jean-Michel, Millet, Pierre, Arnaud, Bernard, Hamel, Christian P.

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RFLP identified by the anonymous DNA segment Ol VII E10 at 18q21.3 (HGM no. D18S8) von MARLHENS, F, DELATTRE, O, BERNARD, A, OLSCHWANG, S, DUTRILLAUX, B, THOMAS, G

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RFLP identified by the anonymous DNA segment OL VII A8 at 18q11 (HGM8 no. D18S7) von DELATTRE, O, BERNARD, A, MARLHENS, F, MONPEZAT, J.-P, DUTRILLAUX, B, THOMAS, G

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Lowered level of translatable messenger RNAs for manganese superoxide dismutase in human fibroblasts transformed by SV 40 von Marlhens, Françoise, Nicole, Annie, Sinet, Pierre-M.

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