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Genomic Patterns of De Novo Mutation in Simplex Autism.
Turner, Tychele N; Coe, Bradley P; Dickel, Diane E; Hoekzema, Kendra; Nelson, Bradley J; Zody, Michael C; Kronenberg, Zev N; Hormozdiari, Fereydoun; Raja, Archana; Pennacchio, Len A; Darnell, Robert B; Eichler, Evan E.
Afiliación
  • Turner TN; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Coe BP; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Dickel DE; Functional Genomics Department, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
  • Hoekzema K; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Nelson BJ; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Zody MC; New York Genome Center, New York, NY 10013, USA.
  • Kronenberg ZN; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Hormozdiari F; Department of Biochemistry and Molecular Medicine, University of California, Davis, Davis, CA 95817, USA.
  • Raja A; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA; Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA.
  • Pennacchio LA; Functional Genomics Department, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA; U.S. Department of Energy Joint Genome Institute, Walnut Creek, CA 94598, USA.
  • Darnell RB; New York Genome Center, New York, NY 10013, USA; Laboratory of Molecular Neuro-Oncology, The Rockefeller University, New York, NY 10065, USA; Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10065, USA.
  • Eichler EE; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA; Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA. Electronic address: eee@gs.washington.edu.
Cell ; 171(3): 710-722.e12, 2017 Oct 19.
Article en En | MEDLINE | ID: mdl-28965761
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno Autístico / Polimorfismo de Nucleótido Simple / Variaciones en el Número de Copia de ADN Límite: Animals / Female / Humans / Male Idioma: En Año: 2017 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno Autístico / Polimorfismo de Nucleótido Simple / Variaciones en el Número de Copia de ADN Límite: Animals / Female / Humans / Male Idioma: En Año: 2017 Tipo del documento: Article