نتائج البحث - Clotilde Penet

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  1. 1
    Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2

    Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2 حسب Alexandra Dürr, C.-S. Davoine, Caroline Paternotte, J. von Fellenberg, S. Cogilnicean, Paula Coutinho, Catherine Lamy, Stéphane Bourgeois, J Prudhomme, Clotilde Penet, J.‐L. Mas, Jean‐Marc Burgunder, Jamïlé Hazan, J. Weissenbach, Alexis Brice, Bertrand Fontaine

    منشور في 1996
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  2. 2
    Germline BAP1 Mutations Predispose to Renal Cell Carcinomas

    Germline BAP1 Mutations Predispose to Renal Cell Carcinomas حسب Tatiana Popova, Lucie Hebert, Virginie Jacquemin, Sophie Gad, Virginie Caux-Moncoutier, C. Dubois-d’Enghien, Bénédicte Richaudeau, Xavier Renaudin, Jason Sellers, Nicolás André, Xavier Sastre‐Garau, Laurence Desjardins, Gàbor Gyapay, Virginie Raynal, Olga M. Sinilnikova, Nadine Andrieu, Élodie Manié, Antoine De Pauw, Paul Gesta, Valérie Bonadona, Christine M. Maugard, Clotilde Penet, Marie‐Françoise Avril, Emmanuel Barillot, Odile Cabaret, Olivier Delattre, Richard J. Kahnoski, Olivier Caron, M. Benfodda, Hui-Han Hu, Nadem Soufir, Brigitte Bressac–de Paillerets, Dominique Stoppa-Lyonnet, Marc‐Henri Stern

    منشور في 2013
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  3. 3
    Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans

    Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans حسب Suzanne Lesage, Étienne Patin, Christel Condroyer, Anne‐Louise Leutenegger, Ebba Lohmann, Nir Giladi, Anat Bar‐Shira, Soraya Belarbi, Nassima Hecham, Pierre Pollak, Anne-Marie Ouvrard-Hernandez, Soraya Bardien, Jonathan Carr, Traki Benhassine, Hiroyuki Tomiyama, Caroline Pirkevi, Tarik Hamadouche, Cécile Cazeneuve, A. Nazlı Başak, Nobutaka Hattori, Alexandra Dürr, Mériem Tazir, Avi Orr‐Urtreger, Lluís Quintana‐Murci, Alexis Brice, Y. Agid, Muriel Bonnet, Michael Borg, Alexis Brice, E. Broussolle, Ph. Damier, A. Destée, Alexandra Dürr, F. Durif, Ebba Lohmann, María Martínez, Clotilde Penet, Pierre Pollak, Olivier Rascol, François Tison, Christine Tranchant, André R. Troiano, Marc Vérin, François Viallet, Marie Vidailhet

    منشور في 2010
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  4. 4
    Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing

    Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing حسب Elodie Girard, Séverine Eon‐Marchais, Robert Olaso, Anne‐Laure Renault, Francesca Damiola, Marie‐Gabrielle Dondon, Laure Barjhoux, Didier Goidin, Vincent Meyer, Dorothée Le Gal, Juana Beauvallet, Noura Mebirouk, Christine Lonjou, Juliette Coignard, Morgane Marcou, Eve Cavaciuti, Céline Baulard, Marie‐Thérèse Bihoreau, Odile Cohen‐Haguenauer, Dominique Leroux, Clotilde Penet, Sandra Fert‐Ferrer, Chrystelle Colas, Thierry Frébourg, François Eisinger, Claude Adenis, Anne Fajac, Laurence Gladieff, Julie Tinat, Anne Floquet, Jean Chiésa, Sophie Giraud, Isabelle Mortemousque, Florent Soubrier, Séverine Audebert‐Bellanger, Jean‐marc Limacher, Christine Lasset, S. Lejeune-Dumoulin, Hélène Dreyfus, Yves‐Jean Bignon, Michel Longy, Pascal Pujol, Laurence Venat‐Bouvet, Valérie Bonadona, Pascaline Berthet, Élisabeth Luporsi, Christine M. Maugard, Catherine Noguès, Capucine Delnatte, Jean‐Pierre Fricker, Paul Gesta, Laurence Faivre, Alain Lortholary, Bruno Buecher, Olivier Caron, Marion Gauthier‐Villars, Isabelle Coupier, Nicolas Servant, Anne Boland, Sylvie Mazoyer, Jean‐François Deleuze, Dominique Stoppa‐Lyonnet, Nadine Andrieu, Fabienne Lesueur

    منشور في 2018
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