Your browser doesn't support javascript.
loading
Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.
Addis, Laura; Ahn, Joo Wook; Dobson, Richard; Dixit, Abhishek; Ogilvie, Caroline M; Pinto, Dalila; Vaags, Andrea K; Coon, Hilary; Chaste, Pauline; Wilson, Scott; Parr, Jeremy R; Andrieux, Joris; Lenne, Bruno; Tumer, Zeynep; Leuzzi, Vincenzo; Aubell, Kristina; Koillinen, Hannele; Curran, Sarah; Marshall, Christian R; Scherer, Stephen W; Strug, Lisa J; Collier, David A; Pal, Deb K.
  • Addis L; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
  • Ahn JW; Neuroscience Discovery Research, Eli Lilly and Company, Erl Wood, Surrey, UK.
  • Dobson R; Department of Cytogenetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Dixit A; Department of Biostatistics and NIHR BRC for Mental Health, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
  • Ogilvie CM; Department of Biostatistics and NIHR BRC for Mental Health, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
  • Pinto D; Department of Cytogenetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Vaags AK; Departments of Psychiatry, and Genetics and Genomic Sciences, Seaver Autism Center, The Mindich Child Health & Development Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Coon H; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Chaste P; Department of Psychiatry, University of Utah School of Medicine, Salt Lake City, Utah.
  • Wilson S; Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Parr JR; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
  • Andrieux J; Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia.
  • Lenne B; School of Medicine and Pharmacology, University of Western Australia, Nedlands, Western Australia, Australia.
  • Tumer Z; Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK.
  • Leuzzi V; Institut de Génétique Médicale, Hopital Jeanne de Flandre, CHRU de Lille, France.
  • Aubell K; Centre de Génétique Chromosomique, GHICL, Hôpital Saint Vincent de Paul, Lille, France.
  • Koillinen H; Applied Human Molecular Genetics, Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Curran S; Department of Pediatrics, Child Neurology and Psychiatry, Sapienza Università di Roma, Rome, Italy.
  • Marshall CR; Institute of Human Genetics, Medical University of Graz, Graz, Austria.
  • Scherer SW; Department of Clinical Genetics, Helsinki University Hospital, Helsinki, Finland.
  • Strug LJ; Department of Cytogenetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Collier DA; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Pal DK; Department of Molecular Genetics, Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
Hum Mutat ; 36(9): 842-50, 2015 Sep.
Article en En | MEDLINE | ID: mdl-26010655
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Eliminación de Secuencia / Estudios de Asociación Genética / Trastorno del Espectro Autista / Trastornos del Lenguaje / Discapacidad Intelectual / Proteínas del Tejido Nervioso Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Año: 2015 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Eliminación de Secuencia / Estudios de Asociación Genética / Trastorno del Espectro Autista / Trastornos del Lenguaje / Discapacidad Intelectual / Proteínas del Tejido Nervioso Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Año: 2015 Tipo del documento: Article