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Volumn 158, Issue 1-3, 2014, Pages 255-260

The phenotypic manifestations of rare CNVs in schizophrenia

Author keywords

CNV; Copy number variation; Family history; Paternal age; Phenotype; Schizophrenia

Indexed keywords

ADULT; ANCESTRY GROUP; ARTICLE; BIRTH; CLINICAL EVALUATION; CLINICAL FEATURE; CONTROLLED STUDY; COPY NUMBER VARIATION; DISEASE SEVERITY; FAMILY HISTORY; FEMALE; GENE DELETION; GENE EXPRESSION; GENE FREQUENCY; GENE FUNCTION; GENETIC ASSOCIATION; HETEROZYGOTE; HUMAN; INTELLIGENCE QUOTIENT; IRISH (CITIZEN); MAJOR CLINICAL STUDY; MALE; ONSET AGE; OUTCOME ASSESSMENT; PATERNAL AGE; PHENOTYPE; PRIORITY JOURNAL; PROGENY; SCHIZOPHRENIA; SOCIAL COGNITION; SOCIAL STATUS; BRAIN; CAUCASIAN; FAMILY; GENETIC PREDISPOSITION; GENETICS; IRELAND; METABOLISM; STATISTICAL MODEL;

EID: 84925464216     PISSN: 09209964     EISSN: 15732509     Source Type: Journal    
DOI: 10.1016/j.schres.2014.06.016     Document Type: Article
Times cited : (10)

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