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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.
Ching, Michael S L; Shen, Yiping; Tan, Wen-Hann; Jeste, Shafali S; Morrow, Eric M; Chen, Xiaoli; Mukaddes, Nahit M; Yoo, Seung-Yun; Hanson, Ellen; Hundley, Rachel; Austin, Christina; Becker, Ronald E; Berry, Gerard T; Driscoll, Katherine; Engle, Elizabeth C; Friedman, Sandra; Gusella, James F; Hisama, Fuki M; Irons, Mira B; Lafiosca, Tina; LeClair, Elaine; Miller, David T; Neessen, Michael; Picker, Jonathan D; Rappaport, Leonard; Rooney, Cynthia M; Sarco, Dean P; Stoler, Joan M; Walsh, Christopher A; Wolff, Robert R; Zhang, Ting; Nasir, Ramzi H; Wu, Bai-Lin.
Affiliation
  • Ching MS; Division of Developmental Medicine, Children's Hospital Boston, Boston, Massachusetts 02115, USA.
Am J Med Genet B Neuropsychiatr Genet ; 153B(4): 937-47, 2010 Jun 05.
Article in En | MEDLINE | ID: mdl-20468056
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Developmental Disabilities Type of study: Prognostic_studies Limits: Child / Female / Humans / Male Language: En Journal: Am J Med Genet B Neuropsychiatr Genet Journal subject: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Year: 2010 Type: Article Affiliation country: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Developmental Disabilities Type of study: Prognostic_studies Limits: Child / Female / Humans / Male Language: En Journal: Am J Med Genet B Neuropsychiatr Genet Journal subject: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Year: 2010 Type: Article Affiliation country: United States