We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
- Authors
Miller, D T; Shen, Y; Weiss, L A; Korn, J; Anselm, I; Bridgemohan, C; Cox, G F; Dickinson, H; Gentile, J; Harris, D J; Hegde, V; Hundley, R; Khwaja, O; Kothare, S; Luedke, C; Nasir, R; Poduri, A; Prasad, K; Raffalli, P; Reinhard, A; Smith, S E; Sobeih, M M; Soul, J S; Stoler, J; Takeoka, M; Tan, W-H; Thakuria, J; Wolff, R; Yusupov, R; Gusella, J F; Daly, M J; Wu, B-L
- Abstract
Segmental duplications at breakpoints (BP4-BP5) of chromosome 15q13.2q13.3 mediate a recurrent genomic imbalance syndrome associated with mental retardation, epilepsy, and/or electroencephalogram (EEG) abnormalities.
- Publication
Journal of medical genetics, 2009, Vol 46, Issue 4, p242
- ISSN
1468-6244
- Publication type
Journal Article
- DOI
10.1136/jmg.2008.059907