22q11 deletion syndrome: A genetic subtype of schizophrenia

Biological Psychiatry

Volumn 46, Issue 7, 1999, Pages 882-891

  Bassett, Anne S ^a,b   Chow, Eva W C ^a,b  

^a CENTRE FOR ADDICTION AND MENTAL HEALTH   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

Chromosome 22; Genetics; Neurodevelopment; Schizophrenia; Subtype; Velocardiofacial syndrome

Indexed keywords

CHROMOSOME 22; CHROMOSOME DELETION; ENVIRONMENTAL FACTOR; FACIES; GENETIC DISORDER; HUMAN; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; REVIEW; SCHIZOPHRENIA;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; GENETIC PREDISPOSITION TO DISEASE; HUMANS; SCHIZOPHRENIA; SCHIZOPHRENIC PSYCHOLOGY; SYNDROME;

EID: 0032874085     PISSN: 00063223     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-3223(99)00114-6     Document Type: Review

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