Hasil Pencarian - Angelo Valetto

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  1. 1
    Clinical Phenotype of DiGeorge Syndrome with Negative Genetic Tests: A Case of DiGeorge-Like Syndrome?

    Clinical Phenotype of DiGeorge Syndrome with Negative Genetic Tests: A Case of DiGeorge-Like Syndrome? oleh Gianluigi Laccetta, Benedetta Toschi, Antonella Fogli, Veronica Bertini, Angelo Valetto, Rita Consolini

    Diterbitkan 2015-01-01
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  2. 2
    Familial Interstitial 6q23.2 Deletion Including Eya4 Associated With Otofaciocervical Syndrome

    Familial Interstitial 6q23.2 Deletion Including Eya4 Associated With Otofaciocervical Syndrome oleh Simone Gana, Angelo Valetto, Benedetta Toschi, Irene Sardelli, Susanna Cappelli, Diego Peroni, Veronica Bertini

    Diterbitkan 2019-07-01
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  3. 3
    Deletion Extents Are Not the Cause of Clinical Variability in 22q11.2 Deletion Syndrome: Does the Interaction between DGCR8 and miRNA-CNVs Play a Major Role?

    Deletion Extents Are Not the Cause of Clinical Variability in 22q11.2 Deletion Syndrome: Does the Interaction between DGCR8 and miRNA-CNVs Play a Major Role? oleh Angelo Valetto, Veronica Bertini, Alessia Azzarà, Annalisa Legitimo, Roberta Milone, Roberta Battini, Rita Consolini

    Diterbitkan 2017-05-01
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  4. 4
    A 17q duplication prenatally detected

    A 17q duplication prenatally detected oleh Rossella Bruno, Angelo Valetto, Veronica Bertini, Cinzia Cosini, Benedetta Toschi, Caterina Congregati, Simona Rossi, Paolo Simi

    Diterbitkan 2015-06-01
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  5. 5
    Case report: Familial case with autism spectrum and bipolar disorder showing a 20q11.21 microduplication including TM9SF4

    Case report: Familial case with autism spectrum and bipolar disorder showing a 20q11.21 microduplication including TM9SF4 oleh Marly Simoncini, Miriam Violi, Angelo Valetto, Veronica Bertini, Francy Cruz-Sanabria, Leonardo Massoni, Liliana Dell’Osso, Claudia Carmassi

    Diterbitkan 2023-11-01
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  6. 6
    A novel genetic variant in DNAI2 detected by custom gene panel in a newborn with Primary Ciliary Dyskinesia: case report

    A novel genetic variant in DNAI2 detected by custom gene panel in a newborn with Primary Ciliary Dyskinesia: case report oleh Maria Santa Rocca, Gioia Piatti, Angela Michelucci, Raffaella Guazzo, Veronica Bertini, Cinzia Vinanzi, Maria Adelaide Caligo, Angelo Valetto, Carlo Foresta

    Diterbitkan 2020-11-01
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  7. 7
    Sorafenib Induced Complete Cytogenetic and Molecular Response in a Chronic Eosinophilic Leukemia Case with t(12;13) Translocation

    Sorafenib Induced Complete Cytogenetic and Molecular Response in a Chronic Eosinophilic Leukemia Case with t(12;13) Translocation oleh Federica Ricci, Serena Balducci, Francesca Guerrini, Susanna Grassi, Elena Ciabatti, Claudia Baratè, Maria Immacolata Ferreri, Cecilia Giuliani, Angelo Valetto, Mario Petrini, Sara Galimberti

    Diterbitkan 2020-07-01
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  8. 8
    Next generation sequencing technologies for a successful diagnosis in a cold case of Leigh syndrome

    Next generation sequencing technologies for a successful diagnosis in a cold case of Leigh syndrome oleh Paolo Aretini, Chiara Maria Mazzanti, Marco La Ferla, Sara Franceschi, Francesca Lessi, Veronica De Gregorio, Claudia Nesti, Angelo Valetto, Veronica Bertini, Benedetta Toschi, Roberta Battini, Maria Adelaide Caligo

    Diterbitkan 2018-07-01
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  9. 9
    The Polycomb BMI1 Protein Is Co-expressed With CD26+ in Leukemic Stem Cells of Chronic Myeloid Leukemia

    The Polycomb BMI1 Protein Is Co-expressed With CD26+ in Leukemic Stem Cells of Chronic Myeloid Leukemia oleh Sara Galimberti, Susanna Grassi, Susanna Grassi, Claudia Baratè, Francesca Guerrini, Elena Ciabatti, Francesca Perutelli, Federica Ricci, Giada Del Genio, Marina Montali, Serena Barachini, Cecilia Giuliani, Maria Immacolata Ferreri, Angelo Valetto, Elisabetta Abruzzese, Chiara Ippolito, Alessandra Iurlo, Monica Bocchia, Anna Sicuranza, Bruno Martino, Lorenzo Iovino, Gabriele Buda, Serena Salehzadeh, Mario Petrini, Antonello Di Paolo, Letizia Mattii

    Diterbitkan 2018-12-01
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