犬心血管奇形成因学の進歩への期待

高尾 篤良

doi:10.11276/jsvc1984.27.4

犬心血管奇形成因学の進歩への期待

高尾篤良

著者情報

ジャーナルフリー

1994 年 27 巻 1 号 p. 4-8

DOI https://doi.org/10.11276/jsvc1984.27.4

詳細

発行日: 1994 年受付日: - J-STAGE公開日: 2009/09/17 受理日: - 早期公開日: - 改訂日: -
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訂正日: 2009/09/17 訂正理由: - 訂正箇所: PDFファイル訂正内容: -

訂正日: 2009/09/17 訂正理由: - 訂正箇所: 引用文献情報訂正内容: Wrong : 1) Patterson, D. F., Pyle, R. L. and J. W. Buchanan (1972) : Hereditary Cardiovascular Malformations of the Dog. Birth Defects : Original Aarticle Series, Vol. III, No.5, pp. 160-174.
2) Mulvihill, J. J.(1972) : Comments of the Epidemiology of Congenital Heart Disease in Dogs, Birth Defects : Original Article Series. Vol. III, No. 5, pp. 175-177.
3) Taussig, H. B. : World survey of the common cardiac malformations : developmental error or genetic variant. In : Congenital Heart Disease After Surgery, Engle, M.A. and J. Perloff ed., pp. 1-42, York Medical Books, U. S. A. 1983.
4) Van Praagh, R. and A. Takao : Etiology and Morphogenesis of Congenital Heart Diesease. Van Praagh, R. and A. Takao ed., Futura, N. Y., 1980.
5) Nora, J. J. and A. Takao : Congenital Heart Diesease : Causes and Processes, Nora, J. J. and A. Takao ed., Futura, N. Y., 1984.
6) Clark, E. B. and A. Takao : Developmental Cardiology : Morphogenesis and Function, Clark, E. B. and A. Takao ed., Futura, N. Y., 1990.
7) Nora, J. J. and A. Takao(1993) : Causes of Congenital Heart Diesease : Old and New modes, Mechanisms and Models. Am. Heart J., 125, 1409-1419.
8) Patterson, D. F., Pexieder, T., Schnarr, W.R., Navratil, T. and R. Alasili (1993) : A single majorgene defect underlying cardiac conotruncal malformations interferes with myocardial growth during embryonic developments : Studies in the CTD nine of Keeshond Dogs. Am. J. Hum. Genet., 52, 388-397.
9) Burn, J., Takao, A., Wilson, D. and K. Momma(1993) : Conotruncal anomaly face syndrome in associated with a deletion within chromosome 22q11. J. Med. Genet. 30, 822-824.
10) Ewart, A. K., Morris, C. A., Atkinson, D., Jim, W., Sternes, K., Spallone, P., Stock, A. D., Leppert, M. and M. T. Keating (1993) : Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome. Nature Genet., 5, 11-16.
11) Casey, B., Devoto, M., Jones, K. L. and A. Ballabio(1993) : Mapping a gene for familical situs abnormalities to human chromosome Xq24-q27. 1. Nature Genet., 5, 403-407.
12) Basson, C. T., Cowley, G. S., Soloman, S.D., Weissman, B., Poznawski, A. K., Traill, T.A., Seidma, J. G. and C. E. Seidman : The clinical and genetic spectrum of the Holt-Oram Syndrome(Heart-Hand Syndrome). New Engl. J. Med. 330, 885-891.

Right : 1) Patterson, D. F., Pyle, R. L. and J. W. Buchanan (1972) : Hereditary Cardiovascular Malformations of the Dog. Birth Defects : Original Aarticle Series, Vol. III, No.5, pp. 160-174.
2) Mulvihill, J. J.(1972) : Comments of the Epidemiology of Congenital Heart Disease in Dogs, Birth Defects : Original Article Series. Vol. III, No. 5, pp. 175-177.
3) Taussig, H. B. : World survey of the common cardiac malformations : developmental error or genetic variant. In : Congenital Heart Disease After Surgery, Engle, M.A. and J. Perloff ed., pp. 1-42, York Medical Books, U. S. A. 1983.
4) Van Praagh, R. and A. Takao : Etiology and Morphogenesis of Congenital Heart Diesease. Van Praagh, R. and A. Takao ed., Futura, N. Y., 1980.
5) Nora, J. J. and A. Takao : Congenital Heart Diesease : Causes and Processes, Nora, J. J. and A. Takao ed., Futura, N. Y., 1984.
6) Clark, E. B. and A. Takao : Developmental Cardiology : Morphogenesis and Function, Clark, E. B. and A. Takao ed., Futura, N. Y., 1990.
7) Nora, J. J. and A. Takao(1993) : Causes of Congenital Heart Diesease : Old and New modes, Mechanisms and Models. Am. Heart J., 125, 1409-1419.
8) Patterson, D. F., Pexieder, T., Schnarr, W.R., Navratil, T. and R. Alasili (1993) : A single major-gene defect underlying cardiac conotruncal malformations interferes with myocardial growth during embryonic developments : Studies in the CTD nine of Keeshond Dogs. Am. J. Hum. Genet., 52, 388-397.
9) Burn, J., Takao, A., Wilson, D. and K. Momma(1993) : Conotruncal anomaly face syndrome in associated with a deletion within chromosome 22q11. J. Med. Genet. 30, 822-824.
10) Ewart, A. K., Morris, C. A., Atkinson, D., Jim, W., Sternes, K., Spallone, P., Stock, A. D., Leppert, M. and M. T. Keating (1993) : Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome. Nature Genet., 5, 11-16.
11) Casey, B., Devoto, M., Jones, K. L. and A. Ballabio(1993) : Mapping a gene for familical situs abnormalities to human chromosome Xq24-q27. 1. Nature Genet., 5, 403-407.
12) Basson, C. T., Cowley, G. S., Soloman, S.D., Weissman, B., Poznawski, A. K., Traill, T.A., Seidma, J. G. and C. E. Seidman : The clinical and genetic spectrum of the Holt-Oram Syndrome(Heart-Hand Syndrome). New Engl. J. Med. 330, 885-891.

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