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Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome.
Thompson, Carlie A; Karelis, Jason; Middleton, Frank A; Gentile, Karen; Coman, Ioana L; Radoeva, Petya D; Mehta, Rashi; Fremont, Wanda P; Antshel, Kevin M; Faraone, Stephen V; Kates, Wendy R.
Afiliação
  • Thompson CA; Department of Psychiatry and Behavioral Sciences, SUNY Upstate Medical University, Syracuse, New York.
  • Karelis J; Department of Psychiatry and Behavioral Sciences, SUNY Upstate Medical University, Syracuse, New York.
  • Middleton FA; Department of Psychiatry and Behavioral Sciences, SUNY Upstate Medical University, Syracuse, New York.
  • Gentile K; Department of Neuroscience, SUNY Upstate Medical University, Syracuse, New York.
  • Coman IL; Department of Neuroscience, SUNY Upstate Medical University, Syracuse, New York.
  • Radoeva PD; Department of Computer Science, SUNY Oswego, Oswego, New York.
  • Mehta R; Department of Psychiatry, University of Washington, Seattle, Washington.
  • Fremont WP; Department of Radiology, SUNY Upstate Medical University, Syracuse, New York.
  • Antshel KM; Department of Psychiatry and Behavioral Sciences, SUNY Upstate Medical University, Syracuse, New York.
  • Faraone SV; Department of Psychiatry and Behavioral Sciences, SUNY Upstate Medical University, Syracuse, New York.
  • Kates WR; Department of Psychology, Syracuse University, Syracuse, New York.
Am J Med Genet B Neuropsychiatr Genet ; 174(3): 295-314, 2017 Apr.
Article em En | MEDLINE | ID: mdl-28139055
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Anormalidades Múltiplas / Síndrome de DiGeorge / Receptor Nogo 1 Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Assunto da revista: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Ano de publicação: 2017 Tipo de documento: Article País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Anormalidades Múltiplas / Síndrome de DiGeorge / Receptor Nogo 1 Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Assunto da revista: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Ano de publicação: 2017 Tipo de documento: Article País de publicação: Estados Unidos