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Clinical phenotype of the recurrent 1q21.1 copy-number variant.
Bernier, Raphael; Steinman, Kyle J; Reilly, Beau; Wallace, Arianne Stevens; Sherr, Elliott H; Pojman, Nicholas; Mefford, Heather C; Gerdts, Jennifer; Earl, Rachel; Hanson, Ellen; Goin-Kochel, Robin P; Berry, Leandra; Kanne, Stephen; Snyder, LeeAnne Green; Spence, Sarah; Ramocki, Melissa B; Evans, David W; Spiro, John E; Martin, Christa L; Ledbetter, David H; Chung, Wendy K.
Afiliación
  • Bernier R; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, USA.
  • Steinman KJ; Department of Neurology, University of Washington, Seattle, Washington, USA.
  • Reilly B; Lakeside Center for Autism, Issaquah, Washington, USA.
  • Wallace AS; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, USA.
  • Sherr EH; Department of Neurology, University of California San Francisco, San Francisco, California, USA.
  • Pojman N; Department of Neurology, University of California San Francisco, San Francisco, California, USA.
  • Mefford HC; Department of Pediatrics, University of Washington, Seattle, Washington, USA.
  • Gerdts J; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, USA.
  • Earl R; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, USA.
  • Hanson E; Division of Developmental Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Goin-Kochel RP; Harvard Medical School, Boston, Massachusetts, USA.
  • Berry L; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
  • Kanne S; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
  • Snyder LG; Thompson Autism Center, University of Missouri, Columbia, Missouri, USA.
  • Spence S; Division of Developmental Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Ramocki MB; Simons Foundation, New York, New York, USA.
  • Evans DW; Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Spiro JE; Department of Neurology, Texas Children's Hospital, Houston, Texas, USA.
  • Martin CL; Autism & Developmental Medicine Institute, Danville, Pennsylvania, USA.
  • Ledbetter DH; Simons Foundation, New York, New York, USA.
  • Chung WK; Autism & Developmental Medicine Institute, Danville, Pennsylvania, USA.
Genet Med ; 18(4): 341-9, 2016 Apr.
Article en En | MEDLINE | ID: mdl-26066539
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Fenotipo / Cromosomas Humanos Par 1 / Trastornos de los Cromosomas / Variaciones en el Número de Copia de ADN Tipo de estudio: Risk_factors_studies Límite: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Fenotipo / Cromosomas Humanos Par 1 / Trastornos de los Cromosomas / Variaciones en el Número de Copia de ADN Tipo de estudio: Risk_factors_studies Límite: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos