Filtros : "Roberds, S" Limpar

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  • Source: Human Molecular Genetics. Unidade: FM

    Assunto: NEUROLOGIA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      PASSOS-BUENO, Maria Rita et al. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy. Human Molecular Genetics, v. 4 , n. 7 , p. 1163-7, 1995Tradução . . Disponível em: https://doi.org/10.1093/hmg/4.7.1163. Acesso em: 13 nov. 2024.
    • APA

      Passos-Bueno, M. R., Moreira, E. S., Vainzof, M., Chamberlain, J., Marie, S. K. N., Pereira, L., et al. (1995). Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy. Human Molecular Genetics, 4 ( 7 ), 1163-7. doi:10.1093/hmg/4.7.1163
    • NLM

      Passos-Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SKN, Pereira L, Akujama JY, Roberds S, Campbell KP, Zatz M. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy [Internet]. Human Molecular Genetics. 1995 ;4 ( 7 ): 1163-7.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1093/hmg/4.7.1163
    • Vancouver

      Passos-Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SKN, Pereira L, Akujama JY, Roberds S, Campbell KP, Zatz M. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy [Internet]. Human Molecular Genetics. 1995 ;4 ( 7 ): 1163-7.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1093/hmg/4.7.1163
  • Source: Human Molecular 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

      PASSOS-BUENO, Maria Rita et al. Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis. Human Molecular Genetics, v. 2 , n. 11, p. 1945-7, 1993Tradução . . Acesso em: 13 nov. 2024.
    • APA

      Passos-Bueno, M. R., Oliveira, J. R., Bakker, E., Anderson, R. D., Marie, S. K. N., Vainzof, M., et al. (1993). Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis. Human Molecular Genetics, 2 ( 11), 1945-7.
    • NLM

      Passos-Bueno MR, Oliveira JR, Bakker E, Anderson RD, Marie SKN, Vainzof M, Roberds S, Campbell KP, Zatz M. Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis. Human Molecular Genetics. 1993 ;2 ( 11): 1945-7.[citado 2024 nov. 13 ]
    • Vancouver

      Passos-Bueno MR, Oliveira JR, Bakker E, Anderson RD, Marie SKN, Vainzof M, Roberds S, Campbell KP, Zatz M. Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis. Human Molecular Genetics. 1993 ;2 ( 11): 1945-7.[citado 2024 nov. 13 ]

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