Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.

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

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.

Affiliation

Miller DT; Department of Laboratory Medicine, Children's Hospital Boston, 300 Longwood Ave, Boston, Massachusetts 02115, USA.

J Med Genet ; 46(4): 242-8, 2009 Apr.

Article in En | MEDLINE | ID: mdl-18805830

Subject(s)

Autistic Disorder/genetics; Chromosome Aberrations; Chromosomes, Human, Pair 15/genetics; Intellectual Disability/genetics; Adolescent; Autistic Disorder/pathology; Child; Child, Preschool; Chromosome Deletion; Comparative Genomic Hybridization; Female; Gene Duplication; Humans; Infant; Intellectual Disability/pathology; Male; Phenotype; Young Adult

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autistic Disorder / Chromosomes, Human, Pair 15 / Chromosome Aberrations / Intellectual Disability Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: J Med Genet Year: 2009 Type: Article Affiliation country: United States

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