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Volumn 105, Issue 3, 2006, Pages 45-48

The Wisconsin Pediatric Cardiac Registry: A mechanism for exploring etiologies of congenital heart defects

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CARDIOLOGIST; CONGENITAL HEART MALFORMATION; CONTROLLED STUDY; DATA BASE; DISEASE ASSOCIATION; DISEASE REGISTRY; HEREDITY; HUMAN; HUMAN EXPERIMENT; MEDICAL RESEARCH; PATHOPHYSIOLOGY; PATIENT REFERRAL; QUESTIONNAIRE;

EID: 33646681216     PISSN: 10981861     EISSN: 10981861     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (4)

References (17)
  • 1
    • 0041591298 scopus 로고    scopus 로고
    • Etiology of congenital cardiovascular malformation: Epidemiology and genetics
    • Allen H, Cark E, Gutgesell H, Driscoll D, eds. Philadelphia, PA: Lippincott Williams & Wilkins
    • Clark, EB. Etiology of congenital cardiovascular malformation: epidemiology and genetics. In: Allen H, Cark E, Gutgesell H, Driscoll D, eds. Moss and Adams' Heart Disease in Infants, Children and Adolescents. 6th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2001.
    • (2001) Moss and Adams' Heart Disease in Infants, Children and Adolescents. 6th Ed.
    • Clark, E.B.1
  • 3
    • 0014334454 scopus 로고
    • Multifactorial inheritance hypothesis for the etiology of congential heart diseases: The genetic-environmental interaction
    • Nora JJ. Multifactorial inheritance hypothesis for the etiology of congential heart diseases: the genetic-environmental interaction. Circulation. 1968;38:604-617.
    • (1968) Circulation , vol.38 , pp. 604-617
    • Nora, J.J.1
  • 4
    • 0036268078 scopus 로고    scopus 로고
    • Risk factors for cardiovascular malformation-a study based on prospectively collected data
    • Cedergren MI, Selbing AJ, Kallen BA. Risk factors for cardiovascular malformation-a study based on prospectively collected data. Scan. J Work Environ Health. 2002;28(1):12-17.
    • (2002) Scan J Work Environ Health , vol.28 , Issue.1 , pp. 12-17
    • Cedergren, M.I.1    Selbing, A.J.2    Kallen, B.A.3
  • 6
    • 0037144658 scopus 로고    scopus 로고
    • Early signs in cardiac development
    • Zaffran S, Frasch M. Early signs in cardiac development. Circ Res. 2002;91:457-469.
    • (2002) Circ Res , vol.91 , pp. 457-469
    • Zaffran, S.1    Frasch, M.2
  • 7
    • 0042632702 scopus 로고    scopus 로고
    • The developing heart and congenital heart defects: A make or break situation
    • Bruneau BG. The developing heart and congenital heart defects: a make or break situation. Clin Genetics. 2003;63:252-261.
    • (2003) Clin Genetics , vol.63 , pp. 252-261
    • Bruneau, B.G.1
  • 8
    • 16944364984 scopus 로고    scopus 로고
    • X-linked situs abnormalities result from mutations in ZIC3
    • Gebbia M, Ferrero GB, Pilia G, et al. X-linked situs abnormalities result from mutations in ZIC3. Nat Genet. 1997;17:252-254.
    • (1997) Nat Genet , vol.17 , pp. 252-254
    • Gebbia, M.1    Ferrero, G.B.2    Pilia, G.3
  • 9
    • 0034022637 scopus 로고    scopus 로고
    • Mutations in TFAP2B cause Char syndrome: A familial form of patent ductus arteriosus
    • Satoda M, Zhao F, Diaz GA, et al. Mutations in TFAP2B cause Char syndrome: a familial form of patent ductus arteriosus. Nat Genet. 2000;25:42-26.
    • (2000) Nat Genet , vol.25 , pp. 42-26
    • Satoda, M.1    Zhao, F.2    Diaz, G.A.3
  • 10
    • 0030636780 scopus 로고    scopus 로고
    • Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome
    • Basson CT, Bachinsky DR, Lin RC, et al. Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome. Nat Genet. 1997;15:30-35.
    • (1997) Nat Genet , vol.15 , pp. 30-35
    • Basson, C.T.1    Bachinsky, D.R.2    Lin, R.C.3
  • 11
    • 16944364802 scopus 로고    scopus 로고
    • Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: A European collaborative study
    • Ryan AK, Goodski JA, Wilson DI, et al. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. J Med Genet. 1997;34:798-804.
    • (1997) J Med Genet , vol.34 , pp. 798-804
    • Ryan, A.K.1    Goodski, J.A.2    Wilson, D.I.3
  • 12
    • 18544383778 scopus 로고    scopus 로고
    • Down syndrome congenital heart disease: A narrowed region and a candidate gene
    • Barlow GM, Xiao-Ning C, et al. Down syndrome congenital heart disease: a narrowed region and a candidate gene. Genetics Med. 2001;3(2):91-101.
    • (2001) Genetics Med , vol.3 , Issue.2 , pp. 91-101
    • Barlow, G.M.1    Xiao-Ning, C.2
  • 13
    • 0030914459 scopus 로고    scopus 로고
    • Mutations in the human Jagged 1 gene are responsible for Alagille syndrome
    • Oda T, Eklahloun AF, Pike BL, et al. Mutations in the human Jagged 1 gene are responsible for Alagille syndrome. Nat Genet. 1997;16:235-242.
    • (1997) Nat Genet , vol.16 , pp. 235-242
    • Oda, T.1    Eklahloun, A.F.2    Pike, B.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.