SCOPUS 정보 검색 플랫폼

Volumn 32, Issue 3, 2002, Pages 181-198

Differential genetic etiology of reading component processes as a function of IQ

(7) Knopik, Valerie S a Smith, Shelley D b Cardon, Lon c Pennington, Bruce d Gayan, Javier c Olson, Richard K e DeFries, John C e

a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE (United States)

b UNIVERSITY OF NEBRASKA LINCOLN (United States)

c UNIVERSITY OF OXFORD (United Kingdom)

d UNIVERSITY OF DENVER (United States)

e UNIVERSITY OF COLORADO (United States)

Author keywords

Genetics; Linkage analysis; Multiple regression; Quantitative trait loci; Reading disability; Sibling pair studies; Twin studies

Indexed keywords

ARTICLE; CHROMOSOME 6; CHROMOSOME 6P; DYSLEXIA; GENETIC LINKAGE; HERITABILITY; HUMAN; INTELLIGENCE QUOTIENT; LANGUAGE DISABILITY; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; PHONEME; PHONETICS; QUANTITATIVE TRAIT LOCUS; READING; WORD RECOGNITION;

EID: 0036318370 PISSN: 00018244 EISSN: None Source Type: Journal
DOI: 10.1023/A:1016069012111 Document Type: Article

Times cited : (33)

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