Hasil Pencarian - Gervasini Cristina

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  1. 1
    Functional analysis of splicing mutations in exon 7 of <it>NF1 </it>gene

    Functional analysis of splicing mutations in exon 7 of <it>NF1 </it>gene oleh Calvieri Stefano, Torrente Isabella, Guida Valentina, Schirinzi Annalisa, De Luca Alessandro, Bottillo Irene, Gervasini Cristina, Larizza Lidia, Pizzuti Antonio, Dallapiccola Bruno

    Diterbitkan 2007-02-01
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  2. 2
    Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports

    Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports oleh Novelli Antonio, Fedele Luigi, Divizia Maria, Barbano Giancarlo, Frontino Giada, Baban Anwar, Carella Massimo, Gervasini Cristina, Gimelli Stefania, Bernardini Laura, Béna Frédérique, Lalatta Faustina, Miozzo Monica, Dallapiccola Bruno

    Diterbitkan 2009-11-01
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  3. 3
    Rubinstein-Taybi Syndrome: spectrum of <it>CREBBP </it>mutations in Italian patients

    Rubinstein-Taybi Syndrome: spectrum of <it>CREBBP </it>mutations in Italian patients oleh Uzielli Maria, Divizia Maria T, Atzeri Francesca, Giordano Lucio, Colapietro Patrizia, Manzini Stefano, Mottadelli Federica, Castronovo Paola, Gervasini Cristina, Milani Donatella, Bentivegna Angela, Neri Giovanni, Bedeschi Maria F, Faravelli Francesca, Selicorni Angelo, Larizza Lidia

    Diterbitkan 2006-10-01
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  4. 4
    Novel <it>C16orf57 </it>mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations

    Novel <it>C16orf57 </it>mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations oleh Colombo Elisa A, Bazan J Fernando, Negri Gloria, Gervasini Cristina, Elcioglu Nursel H, Yucelten Deniz, Altunay Ilknur, Cetincelik Umram, Teti Anna, Del Fattore Andrea, Luciani Matteo, Sullivan Spencer K, Yan Albert C, Volpi Ludovica, Larizza Lidia

    Diterbitkan 2012-01-01
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