Your browser doesn't support javascript.
loading
The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Hanson, Ellen; Bernier, Raphael; Porche, Ken; Jackson, Frank I; Goin-Kochel, Robin P; Snyder, LeeAnne Green; Snow, Anne V; Wallace, Arianne Stevens; Campe, Katherine L; Zhang, Yuan; Chen, Qixuan; D'Angelo, Debra; Moreno-De-Luca, Andres; Orr, Patrick T; Boomer, K B; Evans, David W; Kanne, Stephen; Berry, Leandra; Miller, Fiona K; Olson, Jennifer; Sherr, Elliot; Martin, Christa L; Ledbetter, David H; Spiro, John E; Chung, Wendy K.
Afiliación
  • Hanson E; Division of Developmental Medicine, Boston Children's Hospital, Boston; Department of Psychiatry, Harvard Medical School, Boston, Massachusetts. Electronic address: ellen.hanson@childrens.harvard.edu.
  • Bernier R; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington.
  • Porche K; Division of Developmental Medicine, Boston Children's Hospital, Boston.
  • Jackson FI; Division of Developmental Medicine, Boston Children's Hospital, Boston.
  • Goin-Kochel RP; Department of Pediatrics, Baylor College of Medicine, Houston, Texas;
  • Snyder LG; Division of Developmental Medicine, Boston Children's Hospital, Boston.
  • Snow AV; Division of Developmental Medicine, Boston Children's Hospital, Boston; Department of Psychiatry, Harvard Medical School, Boston, Massachusetts.
  • Wallace AS; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington.
  • Campe KL; Division of Developmental Medicine, Boston Children's Hospital, Boston.
  • Zhang Y; Department of Biostatistics, Columbia University Mailman School of Public Health, New York, New York.
  • Chen Q; Department of Biostatistics, Columbia University Mailman School of Public Health, New York, New York.
  • D'Angelo D; Department of Biostatistics, Columbia University Mailman School of Public Health, New York, New York.
  • Moreno-De-Luca A; Autism and Developmental Medicine Institute, Geisinger Health System, Danville, Pennsylvania; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania; Department of Radiology, Geisinger Health System, Danville, Pennsylvania;
  • Orr PT; Autism and Developmental Medicine Institute, Geisinger Health System, Danville, Pennsylvania.
  • Boomer KB; Department of Mathematics, Bucknell University, Lewisburg, Pennsylvania;
  • Evans DW; Autism and Developmental Medicine Institute, Geisinger Health System, Danville, Pennsylvania.
  • Kanne S; Thompson Center for Autism and Neurodevelopmental Disorders, University of Missouri, Columbia, Missouri.
  • Berry L; Department of Pediatrics, Baylor College of Medicine, Houston, Texas;
  • Miller FK; Division of Developmental Medicine, Boston Children's Hospital, Boston.
  • Olson J; Division of Developmental Medicine, Boston Children's Hospital, Boston.
  • Sherr E; Department of Neurology, University of California, San Francisco, San Francisco, California.
  • Martin CL; Autism and Developmental Medicine Institute, Geisinger Health System, Danville, Pennsylvania; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania.
  • Ledbetter DH; Autism and Developmental Medicine Institute, Geisinger Health System, Danville, Pennsylvania; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania.
  • Spiro JE; Simons Foundation, New York, New York.
  • Chung WK; Departments of Pediatrics and Medicine, Columbia University, New York, New York.
Biol Psychiatry ; 77(9): 785-93, 2015 May 01.
Article en En | MEDLINE | ID: mdl-25064419
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Cromosomas Humanos Par 16 / Discapacidades del Desarrollo / Deleción Cromosómica / Cognición / Trastornos Mentales Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans Idioma: En Revista: Biol Psychiatry Año: 2015 Tipo del documento: Article
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Cromosomas Humanos Par 16 / Discapacidades del Desarrollo / Deleción Cromosómica / Cognición / Trastornos Mentales Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans Idioma: En Revista: Biol Psychiatry Año: 2015 Tipo del documento: Article