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

Saved in:
Bibliographic Details
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
Description
ISSN:1552-485X
DOI:10.1002/ajmg.b.32627