SCOPUS 정보 검색 플랫폼

Volumn 12, Issue 1, 2002, Pages 35-41

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: Quantitative association analysis and positional candidate genes SEMA4F and OTX1

(7) Francks, Clyde a Fisher, Simon E a Olson, Richard K b Pennington, Bruce F c Smith, Shelley D d DeFries, John C b Monaco, Anthony P a

a UNIVERSITY OF OXFORD (United Kingdom)

b UNIVERSITY OF COLORADO (United States)

c UNIVERSITY OF DENVER (United States)

d UNIVERSITY OF NEBRASKA MEDICAL CENTER (United States)

Author keywords

Dyslexia; Linkage disequilibrium; Microsatellite repeats; Polymorphism; Quantitative trait; Single nucleotide

Indexed keywords

HOMEODOMAIN PROTEIN; MICROSATELLITE DNA; PROTEIN OTX1; SEMAPHORIN; SEMAPHORIN 4F; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ARTICLE; BASE PAIRING; BRAIN DEVELOPMENT; CHILD; CHROMOSOME 2P; CHROMOSOME MAP; DYSLEXIA; EXON; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GROWTH CONE; HETEROZYGOSITY; HUMAN; HUMAN CELL; INTRON; MAJOR CLINICAL STUDY; MICROSATELLITE MARKER; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; QUANTITATIVE GENETICS; QUANTITATIVE TRAIT; QUANTITATIVE TRAIT LOCUS; SINGLE NUCLEOTIDE POLYMORPHISM;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 2; DYSLEXIA; GENETIC PREDISPOSITION TO DISEASE; HOMEODOMAIN PROTEINS; HUMANS; LINKAGE (GENETICS); MEMBRANE PROTEINS; NERVE TISSUE PROTEINS; OTX TRANSCRIPTION FACTORS; TRANSCRIPTION FACTORS;

EID: 0036217207 PISSN: 09558829 EISSN: None Source Type: Journal
DOI: 10.1097/00041444-200203000-00005 Document Type: Article

Times cited : (63)

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