Filtros : "Fougerousse, F" Removido: "FM" Limpar

Filtros



Refine with date range


  • Source: Cell. Unidade: IB

    Assunto: GENÉTICA MÉDICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • 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: 25 jul. 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 jul. 25 ] 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 jul. 25 ] Available from: https://doi.org/10.1016/0092-8674(95)90368-2
  • 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
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • 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: 25 jul. 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 jul. 25 ]
    • 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 jul. 25 ]

Digital Library of Intellectual Production of Universidade de São Paulo     2012 - 2024