Examination of candidate genes in language disorder: A model of genetic association for treatment studies

Mental Retardation and Developmental Disabilities Research Reviews

Volumn 10, Issue 3, 2004, Pages 208-217

  Haines, Jonathan ^a,b   Camarata, Stephen ^a,c  

^a VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^b VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c VANDERBILT UNIVERSITY   (United States)

Author keywords

Genetic association; Genetic association and autism; Language; Language disorders; Language intervention; Treatment efficacy

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR; 4 AMINOBUTYRIC ACID B RECEPTOR; 4 AMINOBUTYRIC ACID RECEPTOR; CELL ADHESION MOLECULE; LAMININ; WNT PROTEIN;

ASPERGER SYNDROME; AUTISM; CHROMOSOME 15Q; CHROMOSOME 16; CHROMOSOME 19Q; CHROMOSOME 7Q; GENE INTERACTION; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENETIC ASSOCIATION; GENETIC SCREENING; HEREDITY; HUMAN; LANGUAGE DISABILITY; PERVASIVE DEVELOPMENTAL DISORDER NOT OTHERWISE SPECIFIED; PHENOTYPE; PRIORITY JOURNAL; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM; SOCIAL DISABILITY; TREATMENT OUTCOME;

AUTISTIC DISORDER; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 19; CHROMOSOMES, HUMAN, PAIR 7; FORECASTING; GENE EXPRESSION; GENETIC SCREENING; HUMANS; LANGUAGE DISORDERS; MODELS, GENETIC; PHENOTYPE; RESEARCH DESIGN; TREATMENT OUTCOME;

EID: 11944272620     PISSN: 10804013     EISSN: None     Source Type: Journal    
DOI: 10.1002/mrdd.20035     Document Type: Review

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