Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22

Molecular Psychiatry

Volumn 8, Issue 2, 2003, Pages 176-185

  Turic, D ^a   Robinson, L ^a   Duke, M ^a   Morris, D W ^a   Webb, V ^a   Hamshere, M ^a   Milham, C ^a   Hopkin, E ^a   Pound, K ^a   Fernando, S ^a   Grierson, A ^a   Easton, M ^a   Williams, N ^a   Van Den Bree, M ^a   Chowdhury, R ^b   Gruen, J ^d   Stevenson, J ^c   Krawcza, M ^a   Owen, M J ^a   O'Donovan, M C ^a   Williams, J ^a   more..

^a CARDIFF UNIVERSITY   (United Kingdom)

^b BABRAHAM INSTITUTE   (United Kingdom)

^c UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^d NONE

Author keywords

Dyslexia; Family based association; Linkage disequilibrium mapping; Reading disability

Indexed keywords

ADOLESCENT; ARTICLE; ATTENTION DEFICIT DISORDER; CHROMOSOME 6P; CONTROLLED STUDY; DYSLEXIA; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENE REPLICATION; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MICROSATELLITE MARKER; PHENOTYPE; PHONETICS; PRIORITY JOURNAL; READING; SCHOOL CHILD;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 6; DYSLEXIA; FAMILY HEALTH; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MICROSATELLITE REPEATS; PHENOTYPE;

EID: 0037219324     PISSN: 13594184     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.mp.4001216     Document Type: Article

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