Your browser doesn't support javascript.
loading
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects.
Zhao, Yingjie; Guo, Tingwei; Fiksinski, Ania; Breetvelt, Elemi; McDonald-McGinn, Donna M; Crowley, Terrence B; Diacou, Alexander; Schneider, Maude; Eliez, Stephan; Swillen, Ann; Breckpot, Jeroen; Vermeesch, Joris; Chow, Eva W C; Gothelf, Doron; Duijff, Sasja; Evers, Rens; van Amelsvoort, Thérèse A; van den Bree, Marianne; Owen, Michael; Niarchou, Maria; Bearden, Carrie E; Ornstein, Claudia; Pontillo, Maria; Buzzanca, Antonino; Vicari, Stefano; Armando, Marco; Murphy, Kieran C; Murphy, Clodagh; Garcia-Minaur, Sixto; Philip, Nicole; Campbell, Linda; Morey-Cañellas, Jaume; Raventos, Jasna; Rosell, Jordi; Heine-Suner, Damian; Shprintzen, Robert J; Gur, Raquel E; Zackai, Elaine; Emanuel, Beverly S; Wang, Tao; Kates, Wendy R; Bassett, Anne S; Vorstman, Jacob A S; Morrow, Bernice E.
Afiliação
  • Zhao Y; Department of Genetics, Albert Einstein College of Medicine, Bronx, New York.
  • Guo T; Department of Genetics, Albert Einstein College of Medicine, Bronx, New York.
  • Fiksinski A; Department of Psychiatry, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Breetvelt E; Department of Psychiatry, Hospital for Sick Children, Toronto, Canada.
  • McDonald-McGinn DM; Department of Psychiatry, Hospital for Sick Children, Toronto, Canada.
  • Crowley TB; Division of Human Genetics, Children's Hospital of Philadelphia and Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Diacou A; Division of Human Genetics, Children's Hospital of Philadelphia and Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Schneider M; Department of Genetics, Albert Einstein College of Medicine, Bronx, New York.
  • Eliez S; Developmental Imaging and Psychopathology Lab, University of Geneva School of Medicine, Geneva, Switzerland.
  • Swillen A; Developmental Imaging and Psychopathology Lab, University of Geneva School of Medicine, Geneva, Switzerland.
  • Breckpot J; Center for Human Genetics, Katholieke Universiteit Leuven (KU Leuven), Leuven, Belgium.
  • Vermeesch J; Center for Human Genetics, Katholieke Universiteit Leuven (KU Leuven), Leuven, Belgium.
  • Chow EWC; Center for Human Genetics, Katholieke Universiteit Leuven (KU Leuven), Leuven, Belgium.
  • Gothelf D; Center for Addiction and Mental Health, University of Toronto, Toronto, Canada.
  • Duijff S; Sackler Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel.
  • Evers R; The Child Psychiatry Division, Edmond and Lily Sapfra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
  • van Amelsvoort TA; Department of Psychiatry, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands.
  • van den Bree M; Department of Psychiatry and Psychology, Maastricht University, Maastricht, The Netherlands.
  • Owen M; Department of Psychiatry and Psychology, Maastricht University, Maastricht, The Netherlands.
  • Niarchou M; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neuroscience, Cardiff University, Cardiff, Wales.
  • Bearden CE; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neuroscience, Cardiff University, Cardiff, Wales.
  • Ornstein C; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neuroscience, Cardiff University, Cardiff, Wales.
  • Pontillo M; Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, Los Angeles, California.
  • Buzzanca A; Department of Psychiatry, Hospital Clinico Universidad de Chile, Santiago, Chile.
  • Vicari S; Child and Adolescence Neuropsychiatry Unit, Department of Neuroscience, Children Hospital Bambino Gesu, Rome, Italy.
  • Armando M; Department of Human Neuroscience, University Sapienza of Rome, Rome, Italy.
  • Murphy KC; Child and Adolescence Neuropsychiatry Unit, Department of Neuroscience, Children Hospital Bambino Gesu, Rome, Italy.
  • Murphy C; Developmental Imaging and Psychopathology Lab, University of Geneva School of Medicine, Geneva, Switzerland.
  • Garcia-Minaur S; Child and Adolescence Neuropsychiatry Unit, Department of Neuroscience, Children Hospital Bambino Gesu, Rome, Italy.
  • Philip N; Department of Psychiatry, Royal College of Surgeons in Ireland, Dublin, Ireland.
  • Campbell L; Department of Psychiatry, King's College London, London, England.
  • Morey-Cañellas J; Section of Clinical Genetics and Dismorphology, Instituto de Genética Médica y Molecular, INGEMM, Hospital Universitario La Paz, Madrid, Spain.
  • Raventos J; Department of Medical Genetics, APHM, MMG, INSERM, Aix-Marseille University, Marseille, France.
  • Rosell J; School of Psychology, University of Newcastle, Newcastle, Australia.
  • Heine-Suner D; Section of Genetics, Hospital Son Espases, Palma, Spain.
  • Shprintzen RJ; Section of Genetics, Hospital Son Espases, Palma, Spain.
  • Gur RE; Section of Genetics, Hospital Son Espases, Palma, Spain.
  • Zackai E; Section of Genetics, Hospital Son Espases, Palma, Spain.
  • Emanuel BS; The Virtual Center for Velo-Cardio-Facial Syndrome and Related Disorders, Syracuse, New York.
  • Wang T; Department of Psychiatry and the Lifespan Brain Institute, Perelman School of Medicine and Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Kates WR; Division of Human Genetics, Children's Hospital of Philadelphia and Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Bassett AS; Division of Human Genetics, Children's Hospital of Philadelphia and Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Vorstman JAS; Department of Epidemiology & Population Health, Albert Einstein College of Medicine, Bronx, New York.
  • Morrow BE; Department of Psychiatry and Behavioral Sciences, and Program in Neuroscience, SUNY Upstate Medical University, Syracuse, New York.
Am J Med Genet A ; 176(10): 2172-2181, 2018 10.
Article em En | MEDLINE | ID: mdl-30289625
Assuntos
Palavras-chave
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: Cromossomos Humanos Par 22 / Deleção Cromossômica / Síndrome de DiGeorge Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 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: Cromossomos Humanos Par 22 / Deleção Cromossômica / Síndrome de DiGeorge Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de publicação: Estados Unidos