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A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity.
Biamino, Elisa; Di Gregorio, Eleonora; Belligni, Elga Fabia; Keller, Roberto; Riberi, Evelise; Gandione, Marina; Calcia, Alessandro; Mancini, Cecilia; Giorgio, Elisa; Cavalieri, Simona; Pappi, Patrizia; Talarico, Flavia; Fea, Antonio M; De Rubeis, Silvia; Cirillo Silengo, Margherita; Ferrero, Giovanni Battista; Brusco, Alfredo.
Afiliação
  • Biamino E; Department of Public Health and Pediatrics, University of Torino, Torino, Italy.
  • Di Gregorio E; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, Torino, Italy.
  • Belligni EF; Department of Public Health and Pediatrics, University of Torino, Torino, Italy.
  • Keller R; Adult Autism Center, ASL TO2, Torino, Italy.
  • Riberi E; Department of Public Health and Pediatrics, University of Torino, Torino, Italy.
  • Gandione M; Department of Neuropsychiatry, University of Torino, Torino, Italy.
  • Calcia A; Department of Medical Sciences, University of Torino, Torino, Italy.
  • Mancini C; Department of Medical Sciences, University of Torino, Torino, Italy.
  • Giorgio E; Department of Medical Sciences, University of Torino, Torino, Italy.
  • Cavalieri S; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, Torino, Italy.
  • Pappi P; Department of Medical Sciences, University of Torino, Torino, Italy.
  • Talarico F; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, Torino, Italy.
  • Fea AM; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, Torino, Italy.
  • De Rubeis S; Department of Surgical Sciences, University of Torino, Torino, Italy.
  • Cirillo Silengo M; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Ferrero GB; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Brusco A; Department of Public Health and Pediatrics, University of Torino, Torino, Italy.
Am J Med Genet B Neuropsychiatr Genet ; 171B(2): 290-9, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26620927
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Transtorno Autístico / Cromossomos Humanos Par 3 / Deleção Cromossômica / Deficiência Intelectual / Obesidade Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Ano de publicação: 2016 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Transtorno Autístico / Cromossomos Humanos Par 3 / Deleção Cromossômica / Deficiência Intelectual / Obesidade Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Ano de publicação: 2016 Tipo de documento: Article