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Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.

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Title: Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.
Authors: 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.; EA7364, RADEME, Université de Lille, Lille, France., Duban-Bedu B; Centre de génétique chromosomique, Hopital Saint-Vincent de Paul, Lille, France., Duelund Hjortshøj T; Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark., Goel H; Hunter Genetics, Waratah, New South Wales, Australia.; University of Newcastle, Callaghan, New South Wales, Australia., Loddo S; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy., Morrogh D; North East Thames Regional Genetics Service Laboratory, London, United Kingdom., Mosca-Boidron AL; Service de Cytogénétique, Plateau technique de Biologie, CHU Dijon, France., Novelli A; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy., Olivier-Faivre L; Centre de référence Anomalies du développement et Syndromes malformatifs, FHU TRANSLAD, CHU Dijon, France., Parker J; North East Thames Regional Genetics Service Laboratory, London, United Kingdom., Parker MJ; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Western Bank, Sheffield, United Kingdom., Patch C; King's College London, Florence Nightingale Faculty of Nursing and Midwifery, London, United Kingdom.; Genomics England, Dawson Hall, Charterhouse Square, London, United Kingdom., Pelling AL; Information Officer, Unique - The Rare Chromosome Disorder Support Group (www.rarechromo.org), The Stables, Station Road West, Oxted, Surrey, United Kingdom., Smol T; Institut de génétique médicale, CHU Lille, Lille, France.; EA7364, RADEME, Université de Lille, Lille, France., Tümer Z; Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark., Vanakker O; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium., van Haeringen A; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., Vanlerberghe C; Service de génétique clinique, CHU Lille, Lille, France.; EA7364, RADEME, Université de Lille, Lille, France., Strydom A; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, United Kingdom.; Department of Forensic and Neurodevelopmental Science, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, London, United Kingdom., Skuse D; Behavioural and Brain Sciences Unit, Institute of Child Health, University College London, London, United Kingdom., Bass N; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, United Kingdom.
Source: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics [Am J Med Genet B Neuropsychiatr Genet] 2018 Jun; Vol. 177 (4), pp. 397-405. Date of Electronic Publication: 2018 Mar 31.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235742 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-485X (Electronic) Linking ISSN: 15524841 NLM ISO Abbreviation: Am J Med Genet B Neuropsychiatr Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.
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  Data: <searchLink fieldCode="AU" term="%22Wolfe+K%22">Wolfe K</searchLink>; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22McQuillin+A%22">McQuillin A</searchLink>; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Alesi+V%22">Alesi V</searchLink>; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Boudry+Labis+E%22">Boudry Labis E</searchLink>; Institut de génétique médicale, CHU Lille, Lille, France.<br /><searchLink fieldCode="AU" term="%22Cutajar+P%22">Cutajar P</searchLink>; Nottinghamshire Healthcare NHS Foundation Trust, Nottingham, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Dallapiccola+B%22">Dallapiccola B</searchLink>; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Dentici+ML%22">Dentici ML</searchLink>; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Dieux-Coeslier+A%22">Dieux-Coeslier A</searchLink>; Service de génétique clinique, CHU Lille, Lille, France.; EA7364, RADEME, Université de Lille, Lille, France.<br /><searchLink fieldCode="AU" term="%22Duban-Bedu+B%22">Duban-Bedu B</searchLink>; Centre de génétique chromosomique, Hopital Saint-Vincent de Paul, Lille, France.<br /><searchLink fieldCode="AU" term="%22Duelund+Hjortshøj+T%22">Duelund Hjortshøj T</searchLink>; Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.<br /><searchLink fieldCode="AU" term="%22Goel+H%22">Goel H</searchLink>; Hunter Genetics, Waratah, New South Wales, Australia.; University of Newcastle, Callaghan, New South Wales, Australia.<br /><searchLink fieldCode="AU" term="%22Loddo+S%22">Loddo S</searchLink>; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Morrogh+D%22">Morrogh D</searchLink>; North East Thames Regional Genetics Service Laboratory, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Mosca-Boidron+AL%22">Mosca-Boidron AL</searchLink>; Service de Cytogénétique, Plateau technique de Biologie, CHU Dijon, France.<br /><searchLink fieldCode="AU" term="%22Novelli+A%22">Novelli A</searchLink>; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Olivier-Faivre+L%22">Olivier-Faivre L</searchLink>; Centre de référence Anomalies du développement et Syndromes malformatifs, FHU TRANSLAD, CHU Dijon, France.<br /><searchLink fieldCode="AU" term="%22Parker+J%22">Parker J</searchLink>; North East Thames Regional Genetics Service Laboratory, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Parker+MJ%22">Parker MJ</searchLink>; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Western Bank, Sheffield, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Patch+C%22">Patch C</searchLink>; King's College London, Florence Nightingale Faculty of Nursing and Midwifery, London, United Kingdom.; Genomics England, Dawson Hall, Charterhouse Square, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Pelling+AL%22">Pelling AL</searchLink>; Information Officer, Unique - The Rare Chromosome Disorder Support Group (www.rarechromo.org), The Stables, Station Road West, Oxted, Surrey, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Smol+T%22">Smol T</searchLink>; Institut de génétique médicale, CHU Lille, Lille, France.; EA7364, RADEME, Université de Lille, Lille, France.<br /><searchLink fieldCode="AU" term="%22Tümer+Z%22">Tümer Z</searchLink>; Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.<br /><searchLink fieldCode="AU" term="%22Vanakker+O%22">Vanakker O</searchLink>; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22van+Haeringen+A%22">van Haeringen A</searchLink>; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Vanlerberghe+C%22">Vanlerberghe C</searchLink>; Service de génétique clinique, CHU Lille, Lille, France.; EA7364, RADEME, Université de Lille, Lille, France.<br /><searchLink fieldCode="AU" term="%22Strydom+A%22">Strydom A</searchLink>; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, United Kingdom.; Department of Forensic and Neurodevelopmental Science, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Skuse+D%22">Skuse D</searchLink>; Behavioural and Brain Sciences Unit, Institute of Child Health, University College London, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Bass+N%22">Bass N</searchLink>; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, United Kingdom.
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