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Volumn 16, Issue 7, 2001, Pages 499-504

Neuropsychiatric genetics: Misclassification in linkage studies of phenotype-genotype research

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CLINICAL RESEARCH; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; DISEASE CLASSIFICATION; ERROR; FAMILY; FEMALE; FOLLOW UP; GENETIC LINKAGE; GENETICS; GENOTYPE; GILLES DE LA TOURETTE SYNDROME; HUMAN; MAJOR CLINICAL STUDY; MALE; MODEL; NEUROPSYCHIATRY; PHENOTYPE; PRIORITY JOURNAL;

EID: 0034909443     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/088307380101600707     Document Type: Article
Times cited : (3)

References (20)
  • 9
    • 0027320812 scopus 로고
    • Associations of disease with genetic markers: Déjà vu all over again
    • (1993) Am J Med Genet , vol.48 , pp. 71-73
    • Kidd, K.K.1
  • 13
    • 0022515798 scopus 로고
    • The inheritance of Gilles de la Tourette's syndrome and associated behaviors. Evidence for autosomal dominant transmission
    • (1986) N Engl J Med , vol.315 , pp. 993-997
    • Pauls, D.L.1    Leckman, J.F.2
  • 18
    • 0033365190 scopus 로고    scopus 로고
    • The Tourette Syndrome Association International Consortium for Genetics: A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome
    • (1999) Am J Hum Genet , vol.65 , pp. 1428-1436


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.