Search Results - Buldrini, Barbara

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  1. 1
    The link between hidradenitis suppurativa and phylloid hypomelanosis in partial trisomy-13 mosaicism: New evidences and further genetic/pathogenetic insights

    The link between hidradenitis suppurativa and phylloid hypomelanosis in partial trisomy-13 mosaicism: New evidences and further genetic/pathogenetic insights by Forconi, Riccardo, Bigoni, Stefania, Pacetti, Lucrezia, Host, Cristina, Schettini, Natale, Zedde, Pierantonia, Buldrini, Barbara, Ferlini, Alessandra, Bettoli, Vincenzo

    Published in Pediatric dermatology
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  2. 2
    A New 3p14.2 Microdeletion in a Patient with Intellectual Disability and Language Impairment: Case Report and Review of the Literature

    A New 3p14.2 Microdeletion in a Patient with Intellectual Disability and Language Impairment: Case Report and Review of the Literature by Parmeggiani, Giulia, Buldrini, Barbara, Fini, Sergio, Ferlini, Alessandra, Bigoni, Stefania

    Published in Molecular syndromology
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  3. 3
    The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders

    The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders by Rizzo, Ambra, Alfei, Enrico, Zibordi, Federica, Saletti, Veronica, Zorzi, Giovanna, Freri, Elena, Estienne, Margherita, Girgenti, Vita, D'Arrigo, Stefano, Esposito, Silvia, Buldrini, Barbara, Moroni, Isabella, Milani, Donatella, Granata, Tiziana, Ardissone, Anna, Eoli, Marica, Molteni, Bruna, Bigoni, Stefania, Pantaleoni, Chiara, Nardocci, Nardo, Sciacca, Francesca Luisa

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  4. 4
    New patients with Temple syndrome caused by 14q32 deletion: Genotype-phenotype correlations and risk of thyroid cancer

    New patients with Temple syndrome caused by 14q32 deletion: Genotype-phenotype correlations and risk of thyroid cancer by Severi, Giulia, Bernardini, Laura, Briuglia, Silvana, Bigoni, Stefania, Buldrini, Barbara, Magini, Pamela, Dentici, Maria L., Cordelli, Duccio M., Arrigo, Teresa, Franzoni, Emilio, Fini, Sergio, Italyankina, Eleonora, Loddo, Italia, Novelli, Antonio, Graziano, Claudio

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  5. 5
    Double Interstitial Deletion of the Long Arm of Chromosome 6 in a Patient with Pierre Robin Sequence, Dysmorphisms, and Severe Developmental Delay

    Double Interstitial Deletion of the Long Arm of Chromosome 6 in a Patient with Pierre Robin Sequence, Dysmorphisms, and Severe Developmental Delay by Parmeggiani, Giulia, Bigoni, Stefania, Buldrini, Barbara, Garani, Giampaolo, Clauser, Luigi, Galiè, Manilo, Ferlini, Alessandra, Fini, Sergio

    Published in Molecular syndromology
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  6. 6
    Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q‐phenotype

    Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q‐phenotype by Sensi, Alberto, Prontera, Paolo, Buldrini, Barbara, Palma, Silvia, Aiello, Vincenzo, Gruppioni, Rita, Calzolari, Elisa, Volinia, Stefano, Martini, Alessandro

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  7. 7
    Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis

    Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis by Prontera, Paolo, Buldrini, Barbara, Aiello, Vincenzo, Gruppioni, Rita, Bonfatti, Alessandra, Venti, Giovanna, Ferlini, Alessandra, Sensi, Alberto, Calzolari, Elisa, Donti, Emilio

    Published in Prenatal diagnosis
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  8. 8
    Cytogenetic and Array CGH Characterization of an Intrachromosomal Complex Rearrangement of 4q in a Patient With a 4q-Phenotype. Commentary

    Cytogenetic and Array CGH Characterization of an Intrachromosomal Complex Rearrangement of 4q in a Patient With a 4q-Phenotype. Commentary by SENSI, Alberto, PRONTERA, Paolo, HATCHWELL, Eli, BULDRINI, Barbara, PALMA, Silvia, AIELLO, Vincenzo, GRUPPIONI, Rita, CALZOLARI, Elisa, VOLINIA, Stefano, MARTINI, Alessandro, TORIELLO, Helga V

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  9. 9
    The link between hidradenitis suppurativa and phylloid hypomelanosis in partial trisomy-13 mosaicism: New evidences and further genetic/pathogenetic insights

    The link between hidradenitis suppurativa and phylloid hypomelanosis in partial trisomy-13 mosaicism: New evidences and further genetic/pathogenetic insights by coni, Riccardo, Bigoni, Stefania, Pacetti, Lucrezia, Host, Cristina, Schettini, Natale, Zedde, Pierantonia, Buldrini, Barbara, Ferlini, Alessandra, Bettoli, Vincenzo

    Published in Pediatric dermatology
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  10. 10
    Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype

    Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype by Sensi, Alberto, Prontera, Paolo, Buldrini, Barbara, Palma, Silvia, Aiello, Vincenzo, Gruppioni, Rita, Calzolari, Elisa, Volinia, Stefano, Martini, Alessandro

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