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Characterization of intellectual disability and autism comorbidity through gene panel sequencing.
Aspromonte, Maria C; Bellini, Mariagrazia; Gasparini, Alessandra; Carraro, Marco; Bettella, Elisa; Polli, Roberta; Cesca, Federica; Bigoni, Stefania; Boni, Stefania; Carlet, Ombretta; Negrin, Susanna; Mammi, Isabella; Milani, Donatella; Peron, Angela; Sartori, Stefano; Toldo, Irene; Soli, Fiorenza; Turolla, Licia; Stanzial, Franco; Benedicenti, Francesco; Marino-Buslje, Cristina; Tosatto, Silvio C E; Murgia, Alessandra; Leonardi, Emanuela.
Afiliación
  • Aspromonte MC; Molecular Genetics of Neurodevelopment, Department of Woman and Child Health, University of Padova, C.so Stati Uniti, 4, Padova, Italy.
  • Bellini M; Fondazione Istituto di Ricerca Pediatrica, Città della Speranza, Padova, Italy.
  • Gasparini A; Molecular Genetics of Neurodevelopment, Department of Woman and Child Health, University of Padova, C.so Stati Uniti, 4, Padova, Italy.
  • Carraro M; Fondazione Istituto di Ricerca Pediatrica, Città della Speranza, Padova, Italy.
  • Bettella E; Department of Biomedical Sciences, University of Padova, Padova, Italy.
  • Polli R; Department of Biomedical Sciences, University of Padova, Padova, Italy.
  • Cesca F; Molecular Genetics of Neurodevelopment, Department of Woman and Child Health, University of Padova, C.so Stati Uniti, 4, Padova, Italy.
  • Bigoni S; Fondazione Istituto di Ricerca Pediatrica, Città della Speranza, Padova, Italy.
  • Boni S; Molecular Genetics of Neurodevelopment, Department of Woman and Child Health, University of Padova, C.so Stati Uniti, 4, Padova, Italy.
  • Carlet O; Fondazione Istituto di Ricerca Pediatrica, Città della Speranza, Padova, Italy.
  • Negrin S; Molecular Genetics of Neurodevelopment, Department of Woman and Child Health, University of Padova, C.so Stati Uniti, 4, Padova, Italy.
  • Mammi I; Fondazione Istituto di Ricerca Pediatrica, Città della Speranza, Padova, Italy.
  • Milani D; Medical Genetics Unit, Ospedale Universitario S. Anna, Ferrara, Italy.
  • Peron A; Medical Genetics Unit, San Martino Hospital, Belluno, Italy.
  • Sartori S; Epilepsy and Child Neurophysiology Unit, Scientific Institute IRCCS E. Medea, Treviso, Italy.
  • Toldo I; Epilepsy and Child Neurophysiology Unit, Scientific Institute IRCCS E. Medea, Treviso, Italy.
  • Soli F; Medical Genetics Unit, Dolo General Hospital, Venezia, Italy.
  • Turolla L; Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, University of Milano, Milan, Italy.
  • Stanzial F; Child Neuropsychiatry Unit, Epilepsy Center, Department of Health Sciences, Santi Paolo-Carlo Hospital, University of Milano, Milano, Italy.
  • Benedicenti F; Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah.
  • Marino-Buslje C; Paediatric Neurology Unit, Department of Woman and Child Health, University Hospital of Padova, Padova, Italy.
  • Tosatto SCE; Paediatric Neurology Unit, Department of Woman and Child Health, University Hospital of Padova, Padova, Italy.
  • Murgia A; Medical Genetics Department, APSS Trento, Trento, Italy.
  • Leonardi E; Medical Genetics Unit, Local Health Authority, Treviso, Italy.
Hum Mutat ; 40(9): 1346-1363, 2019 09.
Article en En | MEDLINE | ID: mdl-31209962
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Biología Computacional / Secuenciación de Nucleótidos de Alto Rendimiento / Trastorno del Espectro Autista / Discapacidad Intelectual Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Año: 2019 Tipo del documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Biología Computacional / Secuenciación de Nucleótidos de Alto Rendimiento / Trastorno del Espectro Autista / Discapacidad Intelectual Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Año: 2019 Tipo del documento: Article