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Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development.
Qiu, Yuqi; Arbogast, Thomas; Lorenzo, Sandra Martin; Li, Hongying; Tang, Shih C; Richardson, Ellen; Hong, Oanh; Cho, Shawn; Shanta, Omar; Pang, Timothy; Corsello, Christina; Deutsch, Curtis K; Chevalier, Claire; Davis, Erica E; Iakoucheva, Lilia M; Herault, Yann; Katsanis, Nicholas; Messer, Karen; Sebat, Jonathan.
Afiliação
  • Qiu Y; Division of Biostatistics and Bioinformatics, Department of Family Medicine and Public Health, University of California, San Diego, La Jolla, CA 92093, USA.
  • Arbogast T; Center for Human Disease Modeling, Duke University, Durham, NC 27701, USA.
  • Lorenzo SM; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, Illkirch, France; Centre National de la Recherche Scientifique, UMR7104, Illkirch, France; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, France.
  • Li H; Division of Biostatistics and Bioinformatics, Department of Family Medicine and Public Health, University of California, San Diego, La Jolla, CA 92093, USA.
  • Tang SC; Department of Psychiatry, University of California, San Diego, La Jolla, CA 92093, USA.
  • Richardson E; Center for Human Disease Modeling, Duke University, Durham, NC 27701, USA.
  • Hong O; Department of Psychiatry, University of California, San Diego, La Jolla, CA 92093, USA.
  • Cho S; Department of Psychiatry, University of California, San Diego, La Jolla, CA 92093, USA.
  • Shanta O; Department of Psychiatry, University of California, San Diego, La Jolla, CA 92093, USA; Department of Electrical Engineering, University of California, San Diego, La Jolla, CA 92093, USA.
  • Pang T; Department of Psychiatry, University of California, San Diego, La Jolla, CA 92093, USA.
  • Corsello C; Department of Psychiatry, University of California, San Diego, La Jolla, CA 92093, USA; Rady Children's Hospital, San Diego, CA 92123, USA.
  • Deutsch CK; Eunice Kennedy Shriver Center UMMS, Charlestown and Worcester, MA, USA.
  • Chevalier C; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, Illkirch, France; Centre National de la Recherche Scientifique, UMR7104, Illkirch, France; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, France.
  • Davis EE; Center for Human Disease Modeling, Duke University, Durham, NC 27701, USA.
  • Iakoucheva LM; Department of Psychiatry, University of California, San Diego, La Jolla, CA 92093, USA.
  • Herault Y; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, Illkirch, France; Centre National de la Recherche Scientifique, UMR7104, Illkirch, France; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, France.
  • Katsanis N; Center for Human Disease Modeling, Duke University, Durham, NC 27701, USA.
  • Messer K; Division of Biostatistics and Bioinformatics, Department of Family Medicine and Public Health, University of California, San Diego, La Jolla, CA 92093, USA.
  • Sebat J; Department of Psychiatry, University of California, San Diego, La Jolla, CA 92093, USA; Beyster Center for Genomics of Psychiatric Diseases, University of California, San Diego, La Jolla, CA 92093, USA; Institute for Genomic Medicine, University of California, San Diego, La Jolla, CA 92093, USA; Dep
Cell Rep ; 28(13): 3320-3328.e4, 2019 09 24.
Article em En | MEDLINE | ID: mdl-31553903
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Autístico / Anormalidades Craniofaciais / Transtornos Cromossômicos / Variações do Número de Cópias de DNA / Deficiência Intelectual Limite: Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Autístico / Anormalidades Craniofaciais / Transtornos Cromossômicos / Variações do Número de Cópias de DNA / Deficiência Intelectual Limite: Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article