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Mutations in KCTD1 cause scalp-ear-nipple syndrome

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第一作者: Marneros,A.G.
作者单位: Clinical Genetics Center, Department of Morphology and Genetics, Universidade Federal de S?o Paulo [1] Department of Genetics and Molecular Medicine, University of Florence, Florence 50132, Italy [2] Cutaneous Biology Research Center, Massachusetts General Hospital, Charlestown, MA 02129, United [3] Department of Reconstructive Sciences, University of Connecticut Health Center, Farmington, CT [4] Institut National de la Santé et de la Recherche Médicale U781, Département de Génétique, H?pital [5] Departament of Internal Medicine, Pontifícia Universidade Católica Do Paraná, Curitiba 1155, Brazil [6] Treuman-Katz Center for Pediatric Bioethics, Seattle Children's Research Institute, Seattle, WA [7] Genetics of Learning Disabilities Service, Hunter Genetics, Newcastle, NSW 2298, Australia [8] Department of Plastic and Oral Surgery, Boston Children's Hospital, Boston, MA 02115, United States [9] McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, School of Medicine [10] Department of Genome Sciences, University of Washington, Seattle, WA 98195, United States [11] South East of Scotland Clinical Genetic Service, Western General Hospital, Edinburgh EH4 2XU [12] Department of Pediatrics, University of Washington, Seattle, WA 98195, United States [13] Department of Pediatrics, University of Washington, Seattle, WA 98195, United States, Department of [14] School of Medicine, University of Western Sydney, Campbelltown, NSW 2560, Australia [15] Service de Génétique, Centre Hospitalier Universitaire de Caen, H?pital de la C?te de Nacre, Caen [16]
发布时间 2013-11-20
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The American Journal of Human Genetics

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