Treffer 1 - 6 von 6 für Suche 'Bodereau, Virginie', Suchdauer: 0,53s Treffer weiter einschränken
  1. 1
    Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness

    Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness von Pingault, Veronique, Bodereau, Virginie, Baral, Viviane, Marcos, Severine, Watanabe, Yuli, Chaoui, Asma, Fouveaut, Corinne, Leroy, Chrystel, Vérier-Mine, Odile, Francannet, Christine, Dupin-Deguine, Delphine, Archambeaud, Françoise, Kurtz, François-Joseph, Young, Jacques, Bertherat, Jérôme, Marlin, Sandrine, Goossens, Michel, Hardelin, Jean-Pierre, Dodé, Catherine, Bondurand, Nadege


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  2. 2
    A high level of Hb F unmasks a new case of Hb Wanjiang (β (F3-F4) Ala87_Thr88delinsSer_Gln (HBB:c.255_264 delinsTTTTTCTCAG)) in a pregnant woman of African ancestry

    A high level of Hb F unmasks a new case of Hb Wanjiang (β (F3-F4) Ala87_Thr88delinsSer_Gln (HBB:c.255_264 delinsTTTTTCTCAG)) in a pregnant woman of African ancestry von Pissard, Serge, Moyrand, Claire Bobrie, Peron, Anne, Bodereau, Virginie, Bichr, Allaf, El Osta, Marven, Gouriou, Yann, Ducoroy, Patrick, Wajcman, Henri


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  3. 3
    Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes

    Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes von LEGER, Sandy, BALGUERIE, Xavier, JAMIESON, Robyn V, KRAUSE, Amanda, HONGSHENG CHEN, BAUMANN, Clarisse, NUNES, Luis, DOLLFUS, Helene, GOOSSENS, Michel, PINGAULT, Véronique, GOLDENBERG, Alice, DROUIN-GARRAUD, Valérie, CABOT, Annick, AMSTUTZ-MONTADERT, Isabelle, YOUNG, Paul, JOLY, Pascal, BODEREAU, Virginie, HOLDER-ESPINASSE, Muriel


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  4. 4
    KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndrome

    KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndrome von Drévillon, Loïc, Megarbane, André, Demeer, Bénédicte, Matar, Corine, Benit, Paule, Briand-Suleau, Audrey, Bodereau, Virginie, Ghoumid, Jamal, Nasser, Mayssa, Decrouy, Xavier, Doco-Fenzy, Martine, Rustin, Pierre, Gaillard, Dominique, Goossens, Michel, Giurgea, Irina

    Veröffentlicht in Human molecular genetics

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  5. 5
    Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes: Non-truncating mutations of the MITF basic domain

    Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes: Non-truncating mutations of the MITF... von Léger, Sandy, Balguerie, Xavier, Goldenberg, Alice, Drouin-Garraud, Valérie, Cabot, Annick, Amstutz-Montadert, Isabelle, Young, Paul, Joly, Pascal, Bodereau, Virginie, Holder-Espinasse, Muriel, Jamieson, Robyn V., Krause, Amanda, Chen, Hongsheng, Baumann, Clarisse, Nunes, Luis, Dollfus, Hélène, Goossens, Michel, Pingault, Véronique


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  6. 6
    A high level of Hb F unmasks a new case of Hb Wanjiang (β (F3-F4) Ala87_Thr88delinsSer_Gln (HBB:c.255_264 delinsTTTTTCTCAG)) in a pregnant woman of African ancestry

    A high level of Hb F unmasks a new case of Hb Wanjiang (β (F3-F4) Ala87_Thr88delinsSer_Gln (HBB:c.255_264 delinsTTTTTCTCAG)) in a pregnant woman of African ancestry von Pissard, Serge, Moyrand, Claire Bobrie, Peron, Anne, Bodereau, Virginie, Bichr, Allaf, El Osta, Marven, Gouriou, Yann, Ducoroy, Patrick, Wajcman, Henri


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