Showing 1 - 3 results of 3 for search 'Alberto Sensi', query time: 0.02s Refine Results
  1. 1
    MED12 Mutation in Two Families with X-Linked Ohdo Syndrome

    MED12 Mutation in Two Families with X-Linked Ohdo Syndrome by Luca Rocchetti, Eloisa Evangelista, Luigia De Falco, Giovanni Savarese, Pasquale Savarese, Raffaella Ruggiero, Luigi D’Amore, Alberto Sensi, Antonio Fico

    Published 2021-08-01
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    Article
  2. 2
    Deciphering the pathogenesis of the COL4‐related hematuric nephritis: A genotype/phenotype study

    Deciphering the pathogenesis of the COL4‐related hematuric nephritis: A genotype/phenotype study by Vera Uliana, Paola Sebastio, Matteo Riva, Diana Carli, Claudio Ruberto, Laura Bianchi, Claudio Graziano, Irene Capelli, Flavio Faletra, Roberto Pillon, Teresa Mattina, Alberto Sensi, Francesco Bonatti, Antonio Percesepe

    Published 2021-02-01
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  3. 3
    Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations

    Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy N... by Anna Morgan, Stefania Lenarduzzi, Stefania Cappellani, Vanna Pecile, Marcello Morgutti, Eva Orzan, Sara Ghiselli, Umberto Ambrosetti, Marco Brumat, Poornima Gajendrarao, Martina La Bianca, Flavio Faletra, Enrico Grosso, Fabio Sirchia, Alberto Sensi, Claudio Graziano, Marco Seri, Paolo Gasparini, Paolo Gasparini, Giorgia Girotto, Giorgia Girotto

    Published 2018-12-01
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