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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders

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第一作者: Ching,M.S.L.
作者单位: Harvard Medical School, Boston, MA, United States, Departments of Laboratory Medicine and Pathology [1] Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI [2] Harvard Medical School, Boston, MA, United States, Center for Human Genetic Research, Massachusetts [3] Istanbul Faculty of Medicine, Department of Child Psychiatry, Istanbul University, Istanbul, Turkey [4] Departments of Laboratory Medicine and Pathology, Children's Hospital Boston, Harvard Medical [5] Harvard Medical School, Boston, MA, United States, Division of Genetics, Children's Hospital Boston [6] Harvard Medical School, Boston, MA, United States, Department of Neurology, Children's Hospital [7] Division of Developmental Medicine, Children's Hospital Boston, Harvard Medical School, 300 [8] Division of Genetics, Children's Hospital Boston, Boston, MA, United States [9] Department of Molecular Immunology, Capital Institute of Pediatrics, Beijing, China [10]
发布时间 2014-03-29
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American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics

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