Your browser doesn't support javascript.
loading
Recurrent copy number variations as risk factors for autism spectrum disorders: analysis of the clinical implications.
Oikonomakis, V; Kosma, K; Mitrakos, A; Sofocleous, C; Pervanidou, P; Syrmou, A; Pampanos, A; Psoni, S; Fryssira, H; Kanavakis, E; Kitsiou-Tzeli, S; Tzetis, M.
Afiliação
  • Oikonomakis V; Department of Medical Genetics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
  • Kosma K; Department of Medical Genetics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
  • Mitrakos A; Department of Medical Genetics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
  • Sofocleous C; Department of Medical Genetics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
  • Pervanidou P; Research Institute for the Study of Genetic and Malignant Diseases in Childhood, "Aghia Sophia" Children's Hospital, Athens, Greece.
  • Syrmou A; 1st Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
  • Pampanos A; Department of Medical Genetics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
  • Psoni S; Department of Medical Genetics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
  • Fryssira H; Department of Genetics, "Alexandra" University Maternal Hospital, Athens, Greece.
  • Kanavakis E; Department of Medical Genetics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
  • Kitsiou-Tzeli S; Department of Medical Genetics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
  • Tzetis M; Department of Medical Genetics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Clin Genet ; 89(6): 708-18, 2016 06.
Article em En | MEDLINE | ID: mdl-26777411

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aberrações Cromossômicas / Análise em Microsséries / Variações do Número de Cópias de DNA / Transtorno do Espectro Autista Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aberrações Cromossômicas / Análise em Microsséries / Variações do Número de Cópias de DNA / Transtorno do Espectro Autista Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article