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Volumn 39, Issue 2, 2002, Pages 125-126

Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families [2]

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; CANADA; CHROMOSOME 2P; DYSLEXIA; FAMILY; GENE FREQUENCY; GENE LOCUS; GENE MAPPING; GENETIC SUSCEPTIBILITY; GENOTYPE; HAPLOTYPE; HUMAN; LETTER; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MICROSATELLITE MARKER; PHENOTYPE; PHONEME; PHONETICS; PRIORITY JOURNAL; PSYCHOMETRY; READING;

EID: 0036168959     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter
Times cited : (68)

References (14)
  • 3
    • 0032231869 scopus 로고    scopus 로고
    • Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set
    • erratum 1999;64:334
    • (1998) Am J Hum Genet , vol.63 , pp. 1448-1456
    • Field, L.L.1    Kaplan, B.J.2
  • 6
    • 2042437650 scopus 로고    scopus 로고
    • Initial sequencing and analysis of the human genome
    • (2001) Nature , vol.409 , pp. 860-921
  • 14
    • 0028877463 scopus 로고
    • Genetic dissection af complex traits: Guidelines for interpreting and reporting linkage results
    • (1995) Nat Genet , vol.11 , pp. 241-247
    • Lander, E.S.1    Kruglyak, L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.