What can we learn from the high rates of schizophrenia in people with 22q11.2 deletion syndrome?

World Psychiatry

Volumn 15, Issue 1, 2016, Pages 23-25

  Owen, Michael J ^a   Doherty, Joanne L ^a  

^a CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ATTENTION DEFICIT DISORDER; AUTISM; CHROMOSOME 22; CHROMOSOME DELETION; CHROMOSOME DELETION 22Q11.2; CLINICAL FEATURE; COGNITIVE DEFECT; COPY NUMBER VARIATION; GENETIC PREDISPOSITION; GENOME ANALYSIS; GENOME SIZE; GENOTYPE ENVIRONMENT INTERACTION; HIGH RISK POPULATION; HUMAN; INTELLECTUAL IMPAIRMENT; NONHUMAN; PHENOTYPIC VARIATION; PLEIOTROPY; PREVALENCE; PRIORITY JOURNAL; REVIEW; SCHIZOPHRENIA;

EID: 84964940159     PISSN: 17238617     EISSN: 20515545     Source Type: Journal    
DOI: 10.1002/wps.20274     Document Type: Review

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