Hasil Pencarian - Giorgio Gimelli

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  1. 1
    Identification of an interstitial 18p11.32-p11.31 duplication including the EMILIN2 gene in a family with porokeratosis of Mibelli.

    Identification of an interstitial 18p11.32-p11.31 duplication including the EMILIN2 gene in a family with porokeratosis of Mibelli. oleh Corrado Occella, Dario Bleidl, Paolo Nozza, Samantha Mascelli, Alessandro Raso, Giorgio Gimelli, Stefania Gimelli, Elisa Tassano

    Diterbitkan 2013-01-01
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  2. 2
    Altered intra-nuclear organisation of heterochromatin and genes in ICF syndrome.

    Altered intra-nuclear organisation of heterochromatin and genes in ICF syndrome. oleh Andrew Jefferson, Stefano Colella, Daniela Moralli, Natalie Wilson, Mohammed Yusuf, Giorgio Gimelli, Jiannis Ragoussis, Emanuela V Volpi

    Diterbitkan 2010-06-01
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  3. 3
    Genotype-Phenotype Correlation of 2q37 Deletions Including NPPC Gene Associated with Skeletal Malformations.

    Genotype-Phenotype Correlation of 2q37 Deletions Including NPPC Gene Associated with Skeletal Malformations. oleh Elisa Tassano, Jens Buttgereit, Michael Bader, Margherita Lerone, Maria Teresa Divizia, Renata Bocciardi, Flavia Napoli, Giovanna Pala, Frédérique Sloan-Béna, Stefania Gimelli, Giorgio Gimelli

    Diterbitkan 2013-01-01
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  4. 4
    Parental imbalances involving chromosomes 15q and 22q may predispose to the formation of de novo pathogenic microdeletions and microduplications in the offspring.

    Parental imbalances involving chromosomes 15q and 22q may predispose to the formation of de novo pathogenic microdeletions and microduplications in the offspring. oleh Valeria Capra, Samantha Mascelli, Maria Luisa Garrè, Paolo Nozza, Carlotta Vaccari, Lara Bricco, Frédérique Sloan-Béna, Stefania Gimelli, Cristina Cuoco, Giorgio Gimelli, Elisa Tassano

    Diterbitkan 2013-01-01
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