Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ

Human Genetics

Volumn 133, Issue 7, 2014, Pages 869-881

  Eicher, John D ^a   Powers, Natalie R ^a   Miller, Laura L ^b   Mueller, Kathryn L ^c,d   Mascheretti, Sara ^e   Marino, Cecilia ^e,f,g   Willcutt, Erik G ^h   DeFries, John C ^h   Olson, Richard K ^h   Smith, Shelley D ⁱ   Pennington, Bruce F ^j   Tomblin, J Bruce ^d   Ring, Susan M ^b   Gruen, Jeffrey R ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF BRISTOL   (United Kingdom)

^c MURDOCH CHILDREN'S RESEARCH INSTITUTE   (Australia)

^d UNIVERSITY OF IOWA   (United States)

^e SCIENTIFIC INSTITUTE   (Italy)

^f CENTRE DE RECHERCHE DE L INSTITUT UNIVERSITAIRE EN SANTÉ MENTALE DE QUÉBEC   (Canada)

^g UNIVERSITÉ LAVAL   (Canada)

^h UNIVERSITY OF COLORADO   (United States)

ⁱ UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

^j UNIVERSITY OF DENVER   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ACOT13 GENE; ARTICLE; C6ORF62 GENE; CHILD; CHROMOSOME 6P; CMAHP GENE; COGNITION; DCDC2 GENE; DYSLEXIA; FAM65B GENE; GENE; GENE EXPRESSION; GENE INTERACTION; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENOTYPE; HAPLOTYPE; HUMAN; KIAA0319 GENE; LANGUAGE DISABILITY; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; PROMOTER REGION; SCHOOL CHILD; TDP2 GENE;

CHILD; CHROMOSOMES, HUMAN, PAIR 6; COLORADO; DYSLEXIA; GENETIC LOCI; GENOTYPE; HAPLOTYPES; HUMANS; INTELLIGENCE TESTS; IOWA; ITALY; LANGUAGE DISORDERS; LINKAGE DISEQUILIBRIUM; LONGITUDINAL STUDIES; MICROTUBULE-ASSOCIATED PROTEINS; NERVE TISSUE PROTEINS; NUCLEAR PROTEINS; PHENOTYPE; PROTEINS; PSEUDOGENES; PSYCHOLOGICAL TESTS; READING; THIOLESTER HYDROLASES; TRANSCRIPTION FACTORS;

EID: 84904125672     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-014-1427-3     Document Type: Article

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