메뉴 건너뛰기




Volumn 6, Issue 4, 1996, Pages 264-271

The mendelian basis of congenital heart defects

Author keywords

Congenital heart defect; Genes; Molecular biology

Indexed keywords


EID: 0001035011     PISSN: 10479511     EISSN: None     Source Type: Journal    
DOI: 10.1017/s1047951100003887     Document Type: Article
Times cited : (8)

References (24)
  • 2
    • 0027154167 scopus 로고
    • Causes of congenital heart diseases: Old and new modes, mechanisms, and models
    • Nora JJ. Causes of congenital heart diseases: Old and new modes, mechanisms, and models. Am Heart J 1993; 125: 1409-1419.
    • (1993) Am Heart J , vol.125 , pp. 1409-1419
    • Nora, J.J.1
  • 3
    • 0014334454 scopus 로고
    • Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. the genetic-environmental interaction
    • Nora JJ. Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction. Circulation 1968: 38: 604-617.
    • (1968) Circulation , vol.38 , pp. 604-617
    • Nora, J.J.1
  • 4
    • 0017840201 scopus 로고
    • The evolution of specific genetic and environmental counseling in congenital heart diseases
    • Nora JJ, Nora AH. The evolution of specific genetic and environmental counseling in congenital heart diseases. Circulation 1978; 57: 205-213.
    • (1978) Circulation , vol.57 , pp. 205-213
    • Nora, J.J.1    Nora, A.H.2
  • 5
    • 0013879530 scopus 로고
    • Familial nature of congenital heart diseases
    • Nora JJ, Meyer TC. Familial nature of congenital heart diseases. Pediatrics 1966; 37: 329-334.
    • (1966) Pediatrics , vol.37 , pp. 329-334
    • Nora, J.J.1    Meyer, T.C.2
  • 6
    • 0015538224 scopus 로고
    • Genetic aspects of congenital heart disease
    • Mori K, Ando M, Takao A. Genetic aspects of congenital heart disease. Japan Circul J 1973; 37: 35-39.
    • (1973) Japan Circul J , vol.37 , pp. 35-39
    • Mori, K.1    Ando, M.2    Takao, A.3
  • 8
    • 0022394786 scopus 로고
    • The etiology of congenital cardiovascular malformations: Observations on genetic risks with implications for further birth defects research
    • Ferencz C. The etiology of congenital cardiovascular malformations: Observations on genetic risks with implications for further birth defects research. J Med 1985; 16: 497-508.
    • (1985) J Med , vol.16 , pp. 497-508
    • Ferencz, C.1
  • 10
    • 0023848717 scopus 로고
    • Update on counseling the family with a first-degree relative with a congenital heart defect
    • Nora JJ, Nora AH. Update on counseling the family with a first-degree relative with a congenital heart defect. Am J Med Genet 1988; 29: 137-142.
    • (1988) Am J Med Genet , vol.29 , pp. 137-142
    • Nora, J.J.1    Nora, A.H.2
  • 11
    • 0027537770 scopus 로고
    • A single major-gene defect underlying cardiac conotruncal malformations interferes with myocardial growth during embryonic development: Studies in the CTD line of keeshond dogs
    • Patterson DF, Pexieder T, Schnarr WR, Navratil T, Alaili R. A single major-gene defect underlying cardiac conotruncal malformations interferes with myocardial growth during embryonic development: Studies in the CTD line of keeshond dogs. Am J Hum Genet 1993; 52: 388-397.
    • (1993) Am J Hum Genet , vol.52 , pp. 388-397
    • Patterson, D.F.1    Pexieder, T.2    Schnarr, W.R.3    Navratil, T.4    Alaili, R.5
  • 13
    • 0028239319 scopus 로고
    • A second-generation study of 427 probands with congenital heart defects and their 837 children
    • Whittemore R, Wells JA, Castellsague X. A second-generation study of 427 probands with congenital heart defects and their 837 children. J Am Coll Cardiol 1994; 23: 1459-1467.
    • (1994) J Am Coll Cardiol , vol.23 , pp. 1459-1467
    • Whittemore, R.1    Wells, J.A.2    Castellsague, X.3
  • 16
    • 0025367690 scopus 로고
    • Genetics of conotruncal malformations: Review of the literature and report of a consanguineous kindred with various conotruncal malformations
    • Rein AJJT, Dollberg S, Gale R. Genetics of conotruncal malformations: Review of the literature and report of a consanguineous kindred with various conotruncal malformations. Am J Med Genet 1990; 36: 353-355.
    • (1990) Am J Med Genet , vol.36 , pp. 353-355
    • Rein, A.J.J.T.1    Dollberg, S.2    Gale, R.3
  • 17
    • 0026725876 scopus 로고
    • Deletions within chromosome 22q11 in familial congenital heart disease
    • Wilson DI, Goodship JA, Burn J, Cross IE, Scambler PJ. Deletions within chromosome 22q11 in familial congenital heart disease. Lancet 1992; 340: 573-575.
    • (1992) Lancet , vol.340 , pp. 573-575
    • Wilson, D.I.1    Goodship, J.A.2    Burn, J.3    Cross, I.E.4    Scambler, P.J.5
  • 19
    • 0028177860 scopus 로고
    • Familial atrioventricular septal defect: Possible genetic mechanisms
    • Kumar A, Williams CA, Victorica BE. Familial atrioventricular septal defect: possible genetic mechanisms. Br Heart J 1994; 71: 79-81.
    • (1994) Br Heart J , vol.71 , pp. 79-81
    • Kumar, A.1    Williams, C.A.2    Victorica, B.E.3
  • 21
    • 0029004022 scopus 로고
    • Familial occurrence of patent ductus arteriosus
    • Sletten LJ, Pierpont MEM. Familial occurrence of patent ductus arteriosus. Am J Med Genet 1995; 57: 27-30.
    • (1995) Am J Med Genet , vol.57 , pp. 27-30
    • Sletten, L.J.1    Pierpont, M.E.M.2
  • 22
    • 0026020269 scopus 로고
    • The Marfan syndrome locus: Confirmation of assignment to chromosome 15 and identification of tightly linked markers at 15q15-q21.3
    • Dietz HC, Pyeritz RE, Hall BD, Cadle RG, Hamosh A, Schwartz J, Meyers DA, Francomano CA. The Marfan syndrome locus: Confirmation of assignment to chromosome 15 and identification of tightly linked markers at 15q15-q21.3. Genomics 1991; 9: 355-361.
    • (1991) Genomics , vol.9 , pp. 355-361
    • Dietz, H.C.1    Pyeritz, R.E.2    Hall, B.D.3    Cadle, R.G.4    Hamosh, A.5    Schwartz, J.6    Meyers, D.A.7    Francomano, C.A.8
  • 23
    • 0027051372 scopus 로고
    • Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, 11q, and 12q
    • Sampson JR, Janssen LAJ, Sandkuijl LA, and the Tuberous Sclerosis Collaborative Group. Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, 11q, and 12q. J Med Genet 1992; 29: 861-866.
    • (1992) J Med Genet , vol.29 , pp. 861-866
    • Sampson, J.R.1    Janssen, L.A.J.2    Sandkuijl, L.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.