Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects

Behavior Genetics

Volumn 41, Issue 1, 2011, Pages 90-104

  Newbury, D F ^a   Paracchini, S ^a   Scerri, T S ^a   Winchester, L ^a   Addis, L ^b   Richardson, Alex J ^c   Walter, J ^c   Stein, J F ^c   Talcott, J B ^d   Monaco, A P ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b KING'S COLLEGE LONDON   (United Kingdom)

^c UNIVERSITY OF OXFORD   (United Kingdom)

^d ASTON UNIVERSITY   (United Kingdom)

Author keywords

Association; Dyslexia; Genetics; Specific language impairment (SLI)

Indexed keywords

ARTICLE; ATP2C2 GENE; C20RF3 GENE; CASE CONTROL STUDY; CHILD; CMIP GENE; CNTNAP2 GENE; CONTROLLED STUDY; DCDC2 GENE; DYSLEXIA; DYX1C1 GENE; GENE; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; HUMAN; KIAA0319 GENE; LANGUAGE ABILITY; LANGUAGE DISABILITY; MAJOR CLINICAL STUDY; MRPL19 GENE; RISK ASSESSMENT; RISK FACTOR; ROBO1 GENE; SPECIFIC LANGUAGE IMPAIRMENT;

5' UNTRANSLATED REGIONS; ALLELES; CARRIER PROTEINS; CASE-CONTROL STUDIES; CHILD; COHORT STUDIES; DYSLEXIA; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOTYPE; HUMANS; LANGUAGE DEVELOPMENT DISORDERS; MALE; MEMBRANE PROTEINS; MICROTUBULE-ASSOCIATED PROTEINS; NERVE TISSUE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK ASSESSMENT;

EID: 79952443636     PISSN: 00018244     EISSN: 15733297     Source Type: Journal    
DOI: 10.1007/s10519-010-9424-3     Document Type: Article

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