Deletions of NRXN1 (Neurexin-1) Predispose to a Wide Spectrum of Developmental Disorders
- Author
- CHING, Michael S. L1 2 ; YIPING SHEN2 3 ; AUSTIN, Christina4 ; BECKER, Ronald E1 2 ; BERRY, Gerard T2 4 ; DRISCOLL, Katherine1 2 ; ENGLE, Elizabeth C10 11 12 2 5 ; FRIEDMAN, Sandra1 2 ; GUSELLA, James F13 2 3 ; HISAMA, Fuki M2 4 ; IRONS, Mira B2 4 ; LAFIOSCA, Tina1 2 ; TAN, Wen-Hann2 4 ; LECLAIR, Elaine1 ; MILLER, David T4 ; NEESSEN, Michael1 ; PICKER, Jonathan D4 ; RAPPAPORT, Leonard1 ; ROONEY, Cynthia M5 ; SARCO, Dean P5 ; STOLER, Joan M4 ; WALSH, Christopher A11 14 4 ; WOLFF, Robert R5 ; JESTE, Shafali S2 5 ; TING ZHANG8 ; NASIR, Ramzi H1 ; WU, Bai-Lin15 7 ; MORROW, Eric M6 ; XIAOLI CHEN7 8 ; MUKADDES, Nahit M9 ; YOO, Seung-Yun4 ; HANSON, Ellen1 2 ; HUNDLEY, Rachel1 2
[1] Division of Developmental Medicine, Children's Hospital Boston, Boston, Massachusetts, United States
[2] Harvard Medical School, Boston, Massachusetts, United States
[3] Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States
[4] Division of Genetics, Children's Hospital Boston, Boston, Massachusetts, United States
[5] Department of Neurology, Children's Hospital Boston, Boston, Massachusetts, United States
[6] Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, Rhode Island, United States
[7] Department of Laboratory Medicine, Children's Hospital Boston, Boston, Massachusetts, United States
[8] Department of Molecular Immunology, Capital Institute of Pediatrics, Beijing, China
[9] Istanbul Faculty of Medicine, Department of Child Psychiatry, Istanbul University, Istanbul, Turkey
[10] Children's Hospital Boston, Howard Hughes Medical Institute, Boston, Massachusetts, United States
[11] Manton Center for Orphan Disease Research, Children's Hospital Boston, Boston, Massachusetts, United States
[12] Department of Ophthalmology, Children's Hospital Boston, Boston, Massachusetts, United States
[13] Department of Genetics, Harvard Medical School, Boston, Massachusetts, United States
[14] Howard Hughes Medical Institute, Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States
[15] Children's Hospital and Institutes of Biomedical Science, Fudan University, Shanghai, China
Children's Hospital Boston Genotype Phenotype Study Group, United States - Source
American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 4, pp 937-947, 11 p ; ref : 1 p.1/4
- Publisher
- Wiley-Liss, Hoboken, NJ
- Publication country
- United States
- Document type
- Article
- Language
- English
- Author keyword
- CNV NRXN1 (neurexin-1) NRXN1 exonic deletions array CGH developmental disorders
- Keyword (fr)
- Arriération mentale Délétion Spectre Trouble du développement Aberration chromosomique Déficience intellectuelle
- Keyword (en)
- Mental retardation Deletion Spectrum Developmental disorder Chromosomal aberration Intellectual deficiency
- Keyword (es)
- Retraso mental Deleción Espectro Trastorno desarrollo Aberración cromosómica Deficiencia intelectual
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B18 Psychopathology. Psychiatry / 002B18C Adult and adolescent clinical studies / 002B18C12 Intellectual deficiency
- Francis
- 770 Psychology. Psychoanalysis. Psychiatry / 770-D Psychopathology. Psychiatry / 770-D03 Adult and adolescent clinical studies / 770-D03L Intellectual deficiency
- Discipline
- Medical genetics Psychopathology. Psychiatry. Clinical psychology
- Origin
- Inist-CNRS
- Database
- FRANCIS ; PASCAL
- INIST identifier
- 22818749
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1002/ajmg.b.31063 
https://dx.doi.org/10.1002/ajmg.b.31063
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