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Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

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第一作者: Cappello,S.
作者单位: Medizinisches Genetisches Zentrum, Munich, Germany [1] Helmholtz Center Munich, German Research Center for Environmental Health, Institute for Stem Cell [2] Human Development Biology Resource, Institute of Child Health, London, United Kingdom [3] North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children National [4] Institut für Klinische Genetik, Technische Universit?t Dresden, Dresden, Germany [5] Department of Women's and Children's Health, Dunedin School of Medicine, University of Otago [6] Department of Obstetrics and Gynecology, Mount Sinai Hospital, Toronto, ON, Canada, Prenatal [7] Centre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, QC, Canada [8] Department of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand [9] Division of Genetics and Molecular Medicine, King's College London School of Medicine, Guy's [10] Department of Clinical Genetics, St. Michael's Hospital, Bristol, United Kingdom [11] Department of Biochemistry, University of Otago, Dunedin, New Zealand [12] Department of Clinical Genetics, Vrije Universiteit Medical Center, Amsterdam, Netherlands [13] Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, ON, Canada, Department of [14] Institute of Fundamental Sciences, Massey University, Palmerston North, New Zealand [15] Department of Obstetrics and Gynecology, Mount Sinai Hospital, Toronto, ON, Canada [16] Centre de Génétique Humaine, Université de Franche-Comté, Besan?on, France [17] South West Thames Regional Genetics Service, St. Georges, NHS Healthcare Trust, London, United [18] Department of Laboratory Medicine and Pathobiology, Mount Sinai Hospital, Toronto, ON, Canada [19] Department of Medical Genetics, University Medical Center, Utrecht, Netherlands [20]
发布时间 2014-07-08
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