22q11 deletion syndrome in adults with Schizophrenia

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 81, Issue 4, 1998, Pages 328-337

  Bassett, Anne S ^a,b   Hodgkinson, Kathy ^a   Chow, Eva W C ^a,b   Correia, Susana ^a   Scutt, Laura E ^a   Weksberg, Rosanna ^c  

^a CENTRE FOR ADDICTION AND MENTAL HEALTH   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

Chromosome 22q11; Genetic syndrome; Psychosis; Schizophrenia; Velocardiofacial syndrome

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; LEARNING DISORDER; MALE; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; SCHIZOIDISM; SCHIZOPHRENIA; VELOCARDIOFACIAL SYNDROME;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 22; FACIES; FEMALE; HUMANS; MALE; PHENOTYPE; SCHIZOPHRENIA; SYNDROME;

GENETTA;

EID: 0032503887     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980710)81:4<328::AID-AJMG10>3.0.CO;2-N     Document Type: Article

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