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The complex behavioral phenotype of 15q13.3 microdeletion syndrome.
Ziats, Mark N; Goin-Kochel, Robin P; Berry, Leandra N; Ali, May; Ge, Jun; Guffey, Danielle; Rosenfeld, Jill A; Bader, Patricia; Gambello, Michael J; Wolf, Varina; Penney, Lynette S; Miller, Ryan; Lebel, Robert Roger; Kane, Jeffrey; Bachman, Kristine; Troxell, Robin; Clark, Gary; Minard, Charles G; Stankiewicz, Pawel; Beaudet, Arthur; Schaaf, Christian P.
Afiliação
  • Ziats MN; Medical Scientist Training Program, Baylor College of Medicine, Houston, Texas, USA.
  • Goin-Kochel RP; Autism Center, Texas Children's Hospital, Houston, Texas, USA.
  • Berry LN; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
  • Ali M; Autism Center, Texas Children's Hospital, Houston, Texas, USA.
  • Ge J; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
  • Guffey D; Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Rosenfeld JA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, Texas, USA.
  • Bader P; Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Gambello MJ; Dan L. Duncan Institute for Clinical and Translational Research, Baylor College of Medicine, Houston, Texas, USA.
  • Wolf V; Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Penney LS; Northeast Indiana Genetics, Fort Wayne, Indiana, USA.
  • Miller R; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Lebel RR; Section of Pediatric Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
  • Kane J; Department of Pediatrics, IWK Health Centre, Halifax, Nova Scotia, Canada.
  • Bachman K; Section of Medical Genetics, Department of Pediatrics, SUNY Upstate Medical University, Syracuse, New York, USA.
  • Troxell R; Section of Medical Genetics, Department of Pediatrics, SUNY Upstate Medical University, Syracuse, New York, USA.
  • Clark G; 'Specially for Children Medical Group, Austin, Texas, USA.
  • Minard CG; Department of Pediatrics, Geisinger Medical Center, Danville, Pennsylvania, USA.
  • Stankiewicz P; University of Missouri, Columbia, Missouri, USA.
  • Beaudet A; Section of Pediatric Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
  • Schaaf CP; Dan L. Duncan Institute for Clinical and Translational Research, Baylor College of Medicine, Houston, Texas, USA.
Genet Med ; 18(11): 1111-1118, 2016 11.
Article em En | MEDLINE | ID: mdl-26963284
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Convulsões / Transtornos Cromossômicos / Disfunção Cognitiva / Transtorno do Espectro Autista / Deficiência Intelectual Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Convulsões / Transtornos Cromossômicos / Disfunção Cognitiva / Transtorno do Espectro Autista / Deficiência Intelectual Idioma: En Ano de publicação: 2016 Tipo de documento: Article