Hakutulokset - Francesca Vitelli

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  1. 1
    Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

    Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways Tekijä Francesca Vitelli, Masae Morishima, Ilaria Taddei, Elizabeth A. Lindsay, Antonio Baldini

    Julkaistu 2002
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  2. 2
    TBX1 is required for inner ear morphogenesis

    TBX1 is required for inner ear morphogenesis Tekijä Francesca Vitelli, Antonella Viola, Masae Morishima, Tiziano Pramparo, Antonio Baldini, Elizabeth Lindsay

    Julkaistu 2003
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  3. 3
    Preserved speech variant is allelic of classic Rett syndrome

    Preserved speech variant is allelic of classic Rett syndrome Tekijä Cristina De Bona, Michele Zappella, Joussef Hayek, Ilaria Meloni, Francesca Vitelli, Mirella Bruttini, Roberto Cusano, Paola Loffredo, Ilaria Longo, Alessandra Renieri

    Julkaistu 2000
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  4. 4
    FACL4, a New Gene Encoding Long-Chain Acyl-CoA Synthetase 4, Is Deleted in a Family with Alport Syndrome, Elliptocytosis, and Mental Retardation

    FACL4, a New Gene Encoding Long-Chain Acyl-CoA Synthetase 4, Is Deleted in a Family with Alport Syndrome, Elliptocytosis, and Mental Retardation Tekijä Monica Piccini, Francesca Vitelli, Mirella Bruttini, Barbara R. Pober, Jón J. Jónsson, Marcello Villanova, Massimo Zollo, Giuseppe Borsani, Andrea Ballabio, Alessandra Renieri

    Julkaistu 1998
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  5. 5
    Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice

    Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice Tekijä Victoria Randall, Karen McCue, Catherine Roberts, Vanessa Kyriakopoulou, Sarah Beddow, Angela N. Barrett, Francesca Vitelli, Katrina Prescott, Charles Shaw‐Smith, Koenraad Devriendt, Erika A. Bosman, Georg Steffes, Karen P. Steel, Subreena Simrick, M. Albert Basson, Elizabeth Illingworth, Peter Scambler

    Julkaistu 2009
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