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A comprehensive molecular study on coffin-siris and nicolaides-baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling

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第一作者: Wieczorek,D.
作者单位: Medical Genetics Unit, Department of Pediatrics, Hospital Clínico Universitario Virgen de la [1] Bioinformatics, Computer Science XI, TU Dortmund, Dortmund, Germany [2] Département de génétique mé dicale, CHRU Amiens, France [3] Child Neuropsychiatry Unit, University Hospital, AOUS, Siena, Italy [4] Cologne Center for Genomics (CCG), University of Cologne, Cologne, Germany [5] Department of MedicalGenetics, TheChildren's Memorial Health Institute, Warsaw, Poland [6] Institute of Medical Genetics, University of Zurich, Schwerzenbach-Zurich, Switzerland [7] Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany, Cologne [8] Department of Medical Surgical and Neurological Sciences, Neurodegenerative Disease Unit [9] Genome Informatics, Institute of Human Genetics, Faculty of Medicine, University of Duisburg-Essen [10] Department of Pediatrics, School ofMedicine, Acibadem University, Istanbul, Turkey, Department of [11] Institut für Humangenetik, Universit?tsklinikum Düsseldorf, Düsseldorf, Germany [12] Department of Genetics, Université Paris Descartes-Sorbonne Paris Cité, Institut Imagine, H?pital [13] Department of Medical Genetics, ULB Center of Human Genetics, Erasme Hospital, Brussels, Belgium [14] Institute of Human Genetics, University of Cologne, Cologne, Germany, Center for Molecular Medicine [15] Département de Géné tique, CHU Bordeaux et Université de Bordeaux, Bordeaux, France [16] Institut für Zellbiologie (Tumorforschung), Universit?tsklinikum Essen, Essen, Germany, Universit?t [17] Institut für Humangenetik, Universit?tsklinikum Essen, Essen, Germany [18] Medical Genetics Department, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey [19] Department of Pediatric Genetics, Ihsan Dogramaci Children's Hospital, Hacettepe University School [20] Department of Pediatric Genetics, Turkey [21] Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, Bergen, Norway [22] Department of Pediatric Genetics, Marmara University Hospital, Istanbul, Turkey [23] Clinica Pediatrica, Policlinico Senese Le Scotte Viale Bracci, Siena, Italy [24] Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy [25] Institut für Klinische Genetik, Technische Universit?t Dresden, Dresden, Germany, Division of Human [26] Medical Genetics Unit, Medical Biotechnology Department, University of Siena, Siena, Italy [27] Department of Human Genetics, Katholieke Universiteit Leuven, Leuven, Belgium [28] Institut für Humangenetik, Christian-Albrechts-Universit?t zuKiel, Kiel, Germany [29] Institut für Humangenetik, Friedrich-Alexander-Universit?t Erlangen-Nürnberg, Erlangen, Germany [30] Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, Netherlands [31] Section of Evolutionary Biology, Department of Biology II, University of Munich LMU, Planegg [32] Department of Genetics, Hospital Universitario Cruces, Vizcaya, Spain [33] Department of Medical Genetics, Faculty of Medicine, Ege University, Izmir, Turkey, Department of [34]
发布时间 2014-03-05
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