Hasil Pencarian - Francesca Faravelli

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  1. 1
    P5CS expression study in a new family with ALDH18A1‐associated hereditary spastic paraplegia SPG9

    P5CS expression study in a new family with ALDH18A1‐associated hereditary spastic paraplegia SPG9 oleh Pamela Magini, Clara Marco‐Marin, Juan M. Escamilla‐Honrubia, Diego Martinelli, Carlo Dionisi-Vici, Francesca Faravelli, Francesca Forzano, Marco Seri, Vicente Rubio, Emanuele Panza

    Diterbitkan 2019-08-01
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  2. 2
    FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the FMR1 Gene

    FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the FMR1 Gene oleh Esperanza Fernández, Esperanza Fernández, Elena Gennaro, Filomena Pirozzi, Filomena Pirozzi, Chiara Baldo, Francesca Forzano, Francesca Forzano, Licia Turolla, Francesca Faravelli, Denise Gastaldo, Domenico Coviello, Marina Grasso, Claudia Bagni, Claudia Bagni, Claudia Bagni, Claudia Bagni

    Diterbitkan 2018-11-01
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  3. 3
    The English National Lynch Syndrome transformation project: an NHS Genomic Medicine Service Alliance (GMSA) programme

    The English National Lynch Syndrome transformation project: an NHS Genomic Medicine Service Alliance (GMSA) programme oleh Frances Elmslie, Anna Kim, Kevin J Monahan, Francesca Faravelli, Fiona Lalloo, David N Church, Jackie Cook, Tracie Miles, Neil Ryan, Steven A Hardy, Sally Lane, Alaa Elghobashy, Laura Monje-Garcia, Adam C Shaw, Simone Gelinas, Adele Tyson, Ruth Armstrong, Frank D McDermott, Valerie Ya Wen Wang

    Diterbitkan 2023-12-01
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