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  1. Jomard, Edme François [Author] ; Rémusat, Abel [Other]; Drovetti, Bernardino [Other]; Eberhart, Jean-Michel [Printer] Debure Frères

    Lettre A M. Abel Remusat, Sur Une Nouvelle Mesure De Coudée, Trouvée A Memphis Par M. Le Chever. Drovetti

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    Paris: De Bure, 1827 ; Paris: Merlin, 1827 ; [Paris]: Eberhart, 1827 ; Online-Ausg., Berlin: Staatsbibliothek zu Berlin - Preußischer Kulturbesitz, 2011

  2. Marlhens, Françoise; Bareil, Corinne; Griffoin, Jean-Michel; Zrenner, Eberhart; Amalric, Pierre; Eliaou, Claudie; Liu, Su-Yan; Harris, Eddie; Redmond, T. Michael; Arnaud, Bernard; Claustres, Mireille; Hamel, Christian P.

    Mutations in RPE65 cause Leber's congenital amaurosis

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    Springer Science and Business Media LLC, 1997

    Published in: Nature Genetics, 17 (1997) 2, Seite 139-141

  3. Brommage, Robert; Desai, Urvi; Revelli, JeanPierre; Donoviel, Dorit B.; Fontenot, Gregory K.; DaCosta, Christopher M.; Smith, Deon D.; Kirkpatrick, Laura L.; Coker, Kenneth J.; Donoviel, Michael S.; Eberhart, Derek E.; Holt, Kathleen H.; Kelly, Michael R.; Paradee, William J.; Philips, Anne V.; Platt, Kenneth A.; Suwanichkul, Adisak; Hansen, Gwenn M.; Sands, Arthur T.; Zambrowicz, Brian P.; Powell, David R.

    High‐throughput Screening of Mouse Knockout Lines Identifies True Lean and Obese Phenotypes

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    Wiley, 2008

    Published in: Obesity, 16 (2008) 10, Seite 2362-2367

  4. Bonnet, Crystel; Riahi, Zied; Chantot-Bastaraud, Sandra; Smagghe, Luce; Letexier, Mélanie; Marcaillou, Charles; Lefèvre, Gaëlle M; Hardelin, Jean-Pierre; El-Amraoui, Aziz; Singh-Estivalet, Amrit; Mohand-Saïd, Saddek; Kohl, Susanne; Kurtenbach, Anne; Sliesoraityte, Ieva; Zobor, Ditta; Gherbi, Souad; Testa, Francesco; Simonelli, Francesca; Banfi, Sandro; Fakin, Ana; Glavač, Damjan; Jarc-Vidmar, Martina; Zupan, Andrej; Battelino, Saba; [...]

    An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

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    Springer Science and Business Media LLC, 2016

    Published in: European Journal of Human Genetics, 24 (2016) 12, Seite 1730-1738