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Volumn 20, Issue 11, 2015, Pages 1366-1372

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTISM; CHILD; CLINICAL EVALUATION; CLINICAL FEATURE; CONTROLLED STUDY; COPY NUMBER VARIATION; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; DISEASE SEVERITY; FEMALE; FUNCTIONAL ASSESSMENT; GAIT DISORDER; GENE EXPRESSION; GENE FREQUENCY; GENETIC ANALYSIS; GENETIC ASSOCIATION; HUMAN; INTELLECTUAL IMPAIRMENT; INTELLIGENCE QUOTIENT; INTERPERSONAL COMMUNICATION; LANGUAGE ABILITY; LANGUAGE DISABILITY; MAJOR CLINICAL STUDY; MALE; MATERNAL AGE; PATERNAL AGE; PHENOTYPIC VARIATION; PRIORITY JOURNAL; SEIZURE; ADOLESCENT; ADULT; AGED; ANALYSIS OF VARIANCE; GENETIC PREDISPOSITION; GENETICS; HANDICAPPED CHILD; MIDDLE AGED; PARENT; PATHOPHYSIOLOGY; PHENOTYPE; PSYCHOLOGICAL RATING SCALE; STATISTICAL MODEL; YOUNG ADULT;

EID: 84946494158     PISSN: 13594184     EISSN: 14765578     Source Type: Journal    
DOI: 10.1038/mp.2014.150     Document Type: Article
Times cited : (29)

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