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Volumn 134, Issue 3, 2007, Pages 818-819

Familial recurrence of discrete membranous subaortic stenosis

Author keywords

[No Author keywords available]

Indexed keywords

AORTA SUBVALVULAR STENOSIS; FAMILIAL DISEASE; GENETIC HETEROGENEITY; HEREDITY; HUMAN; LETTER; PRIORITY JOURNAL; RECURRENT DISEASE;

DISCRETE SUBAORTIC STENOSIS; HUMANS;

EID: 34548130785 PISSN: 00225223 EISSN: None Source Type: Journal
DOI: 10.1016/j.jtcvs.2007.01.095 Document Type: Letter

Times cited : (10)

References (8)

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- Familial membranous subaortic stenosis: review of familial inheritance patterns and case report
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- Fatimi, S.H.¹ Ahmad, U.² Javed, M.A.³ Shamin, S.⁴ Ahmad, R.⁵

2
- 0027195653
- Discrete membranous subaortic stenosis in siblings
- Digilio M.C., Giannotti A., Marino B., Obregon M.G., and Dallapiccola B. Discrete membranous subaortic stenosis in siblings. Eur J Pediatr 152 (1933) 622
- (1933) Eur J Pediatr , vol.152 , pp. 622
- Digilio, M.C.¹ Giannotti, A.² Marino, B.³ Obregon, M.G.⁴ Dallapiccola, B.⁵

3
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- Familial subaortic membranous stenosis
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- (1974) Aust N Z J Med , vol.4 , pp. 576-581
- Gale, A.W.¹ Cartmill, T.B.² Bernstein, L.³

4
- 0021886327
- Familial membranous subaortic stenosis
- Urbach J., Glaser J., Balkin J., Rosenmann D., Levy R., Marin G., et al. Familial membranous subaortic stenosis. Cardiology 72 (1985) 214-217
- (1985) Cardiology , vol.72 , pp. 214-217
- Urbach, J.¹ Glaser, J.² Balkin, J.³ Rosenmann, D.⁴ Levy, R.⁵ Marin, G.⁶

5
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- Familial occurrence of discrete subaortic membrane
- Abdallah H., Toomey K., O'Riordan A.C., Davidson A., and Marks L.A. Familial occurrence of discrete subaortic membrane. Pediatr Cardiol 15 (1994) 198-200
- (1994) Pediatr Cardiol , vol.15 , pp. 198-200
- Abdallah, H.¹ Toomey, K.² O'Riordan, A.C.³ Davidson, A.⁴ Marks, L.A.⁵

6
- 14644441750
- Common arterial trunk associated with a homeodomain mutation of NKX2.6
- Heathcote K., Braybrook C., Abushaban L., Guy M., Khetyar M.E., Patton M.A., et al. Common arterial trunk associated with a homeodomain mutation of NKX2.6. Hum Molec Genet 14 (2005) 585-593
- (2005) Hum Molec Genet , vol.14 , pp. 585-593
- Heathcote, K.¹ Braybrook, C.² Abushaban, L.³ Guy, M.⁴ Khetyar, M.E.⁵ Patton, M.A.⁶

7
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- Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot
- Pizzuti A., Sarkozy A., Newton A.L., Conti E., Flex E., Digilio M.C., et al. Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot. Hum Mutat 22 (2003) 372-377
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8
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- Familial tetralogy of Fallot caused by mutation in the Jagged1 gene
- Eldadah Z.A., Hamosh A., Biery N.J., Montgomery R.A., Duke M., Elkins R., et al. Familial tetralogy of Fallot caused by mutation in the Jagged1 gene. Hum Molec Genet 10 (2001) 163-169
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- Eldadah, Z.A.¹ Hamosh, A.² Biery, N.J.³ Montgomery, R.A.⁴ Duke, M.⁵ Elkins, R.⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.