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Visual perception skills: a comparison between patients with Noonan syndrome and 22q11.2 deletion syndrome.
Piccini, G; Menghini, D; D'Andrea, A; Caciolo, C; Pontillo, M; Armando, M; Perrino, F; Mandolesi, L; Salerni, A; Buzzonetti, L; Digilio, M C; Zampino, G; Tartaglia, M; Benassi, M; Vicari, S; Alfieri, P.
Afiliação
  • Piccini G; Department of Neuroscience, Child Neuropsychiatric Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Menghini D; Department of Neuroscience, Child Neuropsychiatric Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • D'Andrea A; Department of Neuroscience, Imaging and Clinical Sciences, Institute for Advanced Biomedical Technologies, University "G.d'Annunzio", Chieti-Pescara, Italy.
  • Caciolo C; Department of Neuroscience, Child Neuropsychiatric Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Pontillo M; Department of Neuroscience, Child Neuropsychiatric Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Armando M; Department of Neuroscience, Child Neuropsychiatric Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Perrino F; Center for Rare Diseases, Department of Pediatrics, Polo Salute Donna e Bambino, Fondazione Policlinico Universitario A. Gemelli, Catholic University, Rome, Italy.
  • Mandolesi L; Psychology Department, University of Bologna, Bologna, Italy.
  • Salerni A; Institute of Ophthalmology, Catholic University, Rome, Italy.
  • Buzzonetti L; Ophthalmology Department, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Digilio MC; Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Zampino G; Center for Rare Diseases, Department of Pediatrics, Polo Salute Donna e Bambino, Fondazione Policlinico Universitario A. Gemelli, Catholic University, Rome, Italy.
  • Tartaglia M; Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Benassi M; Psychology Department, University of Bologna, Bologna, Italy.
  • Vicari S; Department of Neuroscience, Child Neuropsychiatric Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Alfieri P; Department of Neuroscience, Child Neuropsychiatric Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Genes Brain Behav ; 16(6): 627-634, 2017 07.
Article em En | MEDLINE | ID: mdl-28378436
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Percepção Visual / Síndrome da Deleção 22q11 / Síndrome de Noonan Limite: Child / Female / Humans / Male Idioma: En Revista: Genes Brain Behav Assunto da revista: CIENCIAS DO COMPORTAMENTO / GENETICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Itália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Percepção Visual / Síndrome da Deleção 22q11 / Síndrome de Noonan Limite: Child / Female / Humans / Male Idioma: En Revista: Genes Brain Behav Assunto da revista: CIENCIAS DO COMPORTAMENTO / GENETICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Itália