Filtros : "Broux, O" Limpar

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  • Source: Cell. Unidade: IB

    Assunto: GENÉTICA MÉDICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      RICHARD, I et al. Mutations in the proteolytic enzyme calpain 3 cause lim-girdle muscular dystrophy type 2a. Cell, v. 81, p. 27-40, 1995Tradução . . Disponível em: https://doi.org/10.1016/0092-8674(95)90368-2. Acesso em: 09 nov. 2024.
    • APA

      Richard, I., Broux, O., Allamand, V., Fougerousse, F., Chiannilkulchai, N., Bourg, N., et al. (1995). Mutations in the proteolytic enzyme calpain 3 cause lim-girdle muscular dystrophy type 2a. Cell, 81, 27-40. doi:10.1016/0092-8674(95)90368-2
    • NLM

      Richard I, Broux O, Allamand V, Fougerousse F, Chiannilkulchai N, Bourg N, Brenguier L, Devaud C, Pasturaud P, Roudaut C, Hillaire D. Mutations in the proteolytic enzyme calpain 3 cause lim-girdle muscular dystrophy type 2a [Internet]. Cell. 1995 ;81 27-40.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/0092-8674(95)90368-2
    • Vancouver

      Richard I, Broux O, Allamand V, Fougerousse F, Chiannilkulchai N, Bourg N, Brenguier L, Devaud C, Pasturaud P, Roudaut C, Hillaire D. Mutations in the proteolytic enzyme calpain 3 cause lim-girdle muscular dystrophy type 2a [Internet]. Cell. 1995 ;81 27-40.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/0092-8674(95)90368-2
  • Source: Journal of Medical Genetics. Unidades: IB, FM

    Assunto: GENÉTICA MÉDICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      PASSOS-BUENO, Maria Rita et al. Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families. Journal of Medical Genetics, v. 30, n. 5 , p. 385-7, 1993Tradução . . Disponível em: https://doi.org/10.1136/jmg.30.5.385. Acesso em: 09 nov. 2024.
    • APA

      Passos-Bueno, M. R., Richard, I., Vainzof, M., Fougerousse, F., Weissenbach, J., Broux, O., et al. (1993). Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families. Journal of Medical Genetics, 30( 5 ), 385-7. doi:10.1136/jmg.30.5.385
    • NLM

      Passos-Bueno MR, Richard I, Vainzof M, Fougerousse F, Weissenbach J, Broux O, Cohen D, Akiyama J, Marie SKN, Carvalho AA, Guilherme L. Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families [Internet]. Journal of Medical Genetics. 1993 ;30( 5 ): 385-7.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1136/jmg.30.5.385
    • Vancouver

      Passos-Bueno MR, Richard I, Vainzof M, Fougerousse F, Weissenbach J, Broux O, Cohen D, Akiyama J, Marie SKN, Carvalho AA, Guilherme L. Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families [Internet]. Journal of Medical Genetics. 1993 ;30( 5 ): 385-7.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1136/jmg.30.5.385
  • Source: American Journal of Human Genetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB

    Assunto: GENÉTICA MÉDICA

    How to cite
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    • ABNT

      BECKMANN, J S et al. Genetic heterogeneity of the autosomal recessive form of limb-girdle muscular dystrophy. American Journal of Human Genetics. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 09 nov. 2024. , 1992
    • APA

      Beckmann, J. S., Passos-Bueno, M. R., Hillaire, D., Richard, I., Broux, O., Fougerousse, F., et al. (1992). Genetic heterogeneity of the autosomal recessive form of limb-girdle muscular dystrophy. American Journal of Human Genetics. Instituto de Biociências, Universidade de São Paulo.
    • NLM

      Beckmann JS, Passos-Bueno MR, Hillaire D, Richard I, Broux O, Fougerousse F, Vainzof M, Young K, Weissenbach J, Conneally M, Jackson CE, Zatz M. Genetic heterogeneity of the autosomal recessive form of limb-girdle muscular dystrophy. American Journal of Human Genetics. 1992 ;51( 4 suppl.): 182.[citado 2024 nov. 09 ]
    • Vancouver

      Beckmann JS, Passos-Bueno MR, Hillaire D, Richard I, Broux O, Fougerousse F, Vainzof M, Young K, Weissenbach J, Conneally M, Jackson CE, Zatz M. Genetic heterogeneity of the autosomal recessive form of limb-girdle muscular dystrophy. American Journal of Human Genetics. 1992 ;51( 4 suppl.): 182.[citado 2024 nov. 09 ]
  • Source: Comptes Rendus Academie des Sciences. Serie 3. Unidades: IB, FM

    Assunto: GENÉTICA MÉDICA

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    • ABNT

      BECKMANN, J S et al. Gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage. Comptes Rendus Academie des Sciences. Serie 3, v. 312, p. 141-8, 1991Tradução . . Acesso em: 09 nov. 2024.
    • APA

      Beckmann, J. S., Richard, I., Hillaire, D., Broux, O., Antignac, C., Bois, E., et al. (1991). Gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage. Comptes Rendus Academie des Sciences. Serie 3, 312, 141-8.
    • NLM

      Beckmann JS, Richard I, Hillaire D, Broux O, Antignac C, Bois E, Cann H, Cottingham Junior RW, Feingold N, Feingold J, Kalil Filho JE. Gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage. Comptes Rendus Academie des Sciences. Serie 3. 1991 ;312 141-8.[citado 2024 nov. 09 ]
    • Vancouver

      Beckmann JS, Richard I, Hillaire D, Broux O, Antignac C, Bois E, Cann H, Cottingham Junior RW, Feingold N, Feingold J, Kalil Filho JE. Gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage. Comptes Rendus Academie des Sciences. Serie 3. 1991 ;312 141-8.[citado 2024 nov. 09 ]

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