Chromosome 22q11.2 Interstitial deletions among childhood-onset schizophrenics and 'multidimensionally impaired'

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 81, Issue 1, 1998, Pages 41-43

  Yan, WenLiang ^a   Jacobsen, Leslie K ^a   Krasnewich, Donna M ^a   Guan, Xin Yuan ^b   Lenane, Marge C ^a   Paul, Sharon P ^a   Dalwadi, Harnisha N ^a   Zhang, Hongen ^b   Long, Robert T ^a   Kumra, Sanjiv ^a   Martin, Brian M ^a   Scambler, Peter J ^c   Trent, Jeffrey M ^b   Sidransky, Ellen ^a   Ginns, Edward I ^a   Rapoport, Judith L ^a  

^a NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

Childhood schizophrenia; Chromosome 22; DiGeorge syndrome; Mutation; Psychosis; Velocardiofacial syndrome

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CHROMOSOME 22Q; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC SCREENING; HUMAN; HUMAN CELL; INTERSTITIAL CHROMOSOME DELETION; MAJOR CLINICAL STUDY; ONSET AGE; PRIORITY JOURNAL; SCHIZOPHRENIA; VELOCARDIOFACIAL SYNDROME;

CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FEMALE; GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INTELLIGENCE TESTS; MALE; SCHIZOPHRENIA; SOCIAL ISOLATION;

EID: 0007482654     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980207)81:1<41::AID-AJMG8>3.0.CO;2-Q     Document Type: Article

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