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Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations.
Cárdenas-de-la-Parra, Alonso; Martin-Brevet, Sandra; Moreau, Clara; Rodriguez-Herreros, Borja; Fonov, Vladimir S; Maillard, Anne M; Zürcher, Nicole R; Hadjikhani, Nouchine; Beckmann, Jacques S; Reymond, Alexandre; Draganski, Bogdan; Jacquemont, Sébastien; Collins, D Louis.
Afiliação
  • Cárdenas-de-la-Parra A; Department of Biological and Biomedical Engineering, Montreal Neurological Institute, Montreal, Quebec, Canada.
  • Martin-Brevet S; Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; LREN, Département des neurosciences cliniques, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland.
  • Moreau C; CHU Sainte-Justine Research Center, Université de Montréal, Montréal, QC, Canada.
  • Rodriguez-Herreros B; Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; CHU Sainte-Justine Research Center, Université de Montréal, Montréal, QC, Canada.
  • Fonov VS; Department of Biological and Biomedical Engineering, Montreal Neurological Institute, Montreal, Quebec, Canada.
  • Maillard AM; Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; Centre Cantonal Autisme, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland.
  • Zürcher NR; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  • Hadjikhani N; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA; Gillberg Neuropsychiatry Centre, Göteborg, Sweden.
  • Beckmann JS; Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland.
  • Reymond A; Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
  • Draganski B; LREN, Département des neurosciences cliniques, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; Department of Neurology, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.
  • Jacquemont S; Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; CHU Sainte-Justine Research Center, Université de Montréal, Montréal, QC, Canada. Electronic address: Sebastien.jacquemont@umontreal.ca.
  • Collins DL; Department of Biological and Biomedical Engineering, Montreal Neurological Institute, Montreal, Quebec, Canada.
Neuroimage ; 203: 116155, 2019 12.
Article em En | MEDLINE | ID: mdl-31494251
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 16 / Encéfalo / Deleção Cromossômica / Variações do Número de Cópias de DNA / Duplicação Cromossômica Tipo de estudo: Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Humans Idioma: En Revista: Neuroimage Assunto da revista: DIAGNOSTICO POR IMAGEM Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Canadá
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 16 / Encéfalo / Deleção Cromossômica / Variações do Número de Cópias de DNA / Duplicação Cromossômica Tipo de estudo: Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Humans Idioma: En Revista: Neuroimage Assunto da revista: DIAGNOSTICO POR IMAGEM Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Canadá