Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired".

Yan, W; Jacobsen, L K; Krasnewich, D M; Guan, X Y; Lenane, M C; Paul, S P; Dalwadi, H N; Zhang, H; Long, R T; Kumra, S; Martin, B M; Scambler, P J; Trent, J M; Sidransky, E; Ginns, E I; Rapoport, J L

Yan, W; Jacobsen, L K; Krasnewich, D M; Guan, X Y; Lenane, M C; Paul, S P; Dalwadi, H N; Zhang, H; Long, R T; Kumra, S; Martin, B M; Scambler, P J; Trent, J M; Sidransky, E; Ginns, E I; Rapoport, J L.

Affiliation

Yan W; Child Psychiatry Branch, National Institute of Mental Health, Bethesda, Maryland 20892-4405, USA. wlyan@helix.nih.gov

Am J Med Genet ; 81(1): 41-3, 1998 Feb 07.

Article in En | MEDLINE | ID: mdl-9514586

Subject(s)

Chromosomes, Human, Pair 22; Gene Deletion; Schizophrenia/genetics; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; DiGeorge Syndrome/genetics; Female; Humans; In Situ Hybridization, Fluorescence; Intelligence Tests; Male; Social Isolation

Search on Google

Add to My VHL

XML

PubMed Links

Database: MEDLINE Main subject: Schizophrenia / Chromosomes, Human, Pair 22 / Gene Deletion Type of study: Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Language: En Journal: Am J Med Genet Year: 1998 Type: Article Affiliation country: United States

Search on Google

Add to My VHL

XML

PubMed Links