Your browser doesn't support javascript.
loading
Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.
Wolfe, Kate; McQuillin, Andrew; Alesi, Viola; Boudry Labis, Elise; Cutajar, Peter; Dallapiccola, Bruno; Dentici, Maria Lisa; Dieux-Coeslier, Anne; Duban-Bedu, Benedicte; Duelund Hjortshøj, Tina; Goel, Himanshu; Loddo, Sara; Morrogh, Deborah; Mosca-Boidron, Anne-Laure; Novelli, Antonio; Olivier-Faivre, Laurence; Parker, Jennifer; Parker, Michael J; Patch, Christine; Pelling, Anna L; Smol, Thomas; Tümer, Zeynep; Vanakker, Olivier; van Haeringen, Arie; Vanlerberghe, Clémence; Strydom, Andre; Skuse, David; Bass, Nick.
Afiliación
  • Wolfe K; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, United Kingdom.
  • McQuillin A; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, United Kingdom.
  • Alesi V; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.
  • Boudry Labis E; Institut de génétique médicale, CHU Lille, Lille, France.
  • Cutajar P; Nottinghamshire Healthcare NHS Foundation Trust, Nottingham, United Kingdom.
  • Dallapiccola B; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.
  • Dentici ML; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.
  • Dieux-Coeslier A; Service de génétique clinique, CHU Lille, Lille, France.
  • Duban-Bedu B; EA7364, RADEME, Université de Lille, Lille, France.
  • Duelund Hjortshøj T; Centre de génétique chromosomique, Hopital Saint-Vincent de Paul, Lille, France.
  • Goel H; Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Loddo S; Hunter Genetics, Waratah, New South Wales, Australia.
  • Morrogh D; University of Newcastle, Callaghan, New South Wales, Australia.
  • Mosca-Boidron AL; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.
  • Novelli A; North East Thames Regional Genetics Service Laboratory, London, United Kingdom.
  • Olivier-Faivre L; Service de Cytogénétique, Plateau technique de Biologie, CHU Dijon, France.
  • Parker J; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.
  • Parker MJ; Centre de référence Anomalies du développement et Syndromes malformatifs, FHU TRANSLAD, CHU Dijon, France.
  • Patch C; North East Thames Regional Genetics Service Laboratory, London, United Kingdom.
  • Pelling AL; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Western Bank, Sheffield, United Kingdom.
  • Smol T; King's College London, Florence Nightingale Faculty of Nursing and Midwifery, London, United Kingdom.
  • Tümer Z; Genomics England, Dawson Hall, Charterhouse Square, London, United Kingdom.
  • Vanakker O; Information Officer, Unique - The Rare Chromosome Disorder Support Group (www.rarechromo.org), The Stables, Station Road West, Oxted, Surrey, United Kingdom.
  • van Haeringen A; Institut de génétique médicale, CHU Lille, Lille, France.
  • Vanlerberghe C; EA7364, RADEME, Université de Lille, Lille, France.
  • Strydom A; Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Skuse D; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Bass N; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Am J Med Genet B Neuropsychiatr Genet ; 177(4): 397-405, 2018 06.
Article en En | MEDLINE | ID: mdl-29603867
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 2 / Discapacidades del Desarrollo / Trastornos Mentales Tipo de estudio: Diagnostic_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Asunto de la revista: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 2 / Discapacidades del Desarrollo / Trastornos Mentales Tipo de estudio: Diagnostic_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Asunto de la revista: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido