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Filtros : "Zatz, Mayana" "Financiado pelo PRONEX" Removidos: "FOB-BAO" "jo" "kan" Limpar

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  • Artigo de periodico

    Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype (2004)

    Tonini, M. M. O; Pavanello, R C M; Gurgel-Giannetti, J; Lemmers, R J; Maarel, S M van der; Frants, R R; Zatz, Mayana

    Source: Journal of Medical Genetics. Unidade: IB

    Subjects: GENÉTICA MÉDICA, MALFORMAÇÕES, DOENÇAS MUSCULOSQUELÉTICAS, DISTROFIA MUSCULAR

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

    • ABNT

      TONINI, M. M. O et al. Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype. Journal of Medical Genetics, v. 41, n. 2, 2004Tradução . . Disponível em: https://doi.org/10.1136/jmg.2003.010637. Acesso em: 09 jul. 2024.

    • APA

      Tonini, M. M. O., Pavanello, R. C. M., Gurgel-Giannetti, J., Lemmers, R. J., Maarel, S. M. van der, Frants, R. R., & Zatz, M. (2004). Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype. Journal of Medical Genetics, 41( 2). doi:10.1136/jmg.2003.010637

    • NLM

      Tonini MMO, Pavanello RCM, Gurgel-Giannetti J, Lemmers RJ, Maarel SM van der, Frants RR, Zatz M. Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype [Internet]. Journal of Medical Genetics. 2004 ; 41( 2):[citado 2024 jul. 09 ] Available from: https://doi.org/10.1136/jmg.2003.010637

    • Vancouver

      Tonini MMO, Pavanello RCM, Gurgel-Giannetti J, Lemmers RJ, Maarel SM van der, Frants RR, Zatz M. Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype [Internet]. Journal of Medical Genetics. 2004 ; 41( 2):[citado 2024 jul. 09 ] Available from: https://doi.org/10.1136/jmg.2003.010637

  • Artigo de periodico

    Protein defects in neuromuscular diseases (2003)

    Vainzof, Mariz ; Zatz, Mayana

    Source: Brazilian Journal of Medical and Biological Research. Unidade: IB

    Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES, MUTAÇÃO GENÉTICA, PROTEÍNAS MUSCULARES

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

    • ABNT

      VAINZOF, Mariz e ZATZ, Mayana. Protein defects in neuromuscular diseases. Brazilian Journal of Medical and Biological Research, v. 36, p. 543-555, 2003Tradução . . Disponível em: https://doi.org/10.1590/S0100-879X2003000500001. Acesso em: 09 jul. 2024.

    • APA

      Vainzof, M., & Zatz, M. (2003). Protein defects in neuromuscular diseases. Brazilian Journal of Medical and Biological Research, 36, 543-555. doi:10.1590/S0100-879X2003000500001

    • NLM

      Vainzof M, Zatz M. Protein defects in neuromuscular diseases [Internet]. Brazilian Journal of Medical and Biological Research. 2003 ; 36 543-555.[citado 2024 jul. 09 ] Available from: https://doi.org/10.1590/S0100-879X2003000500001

    • Vancouver

      Vainzof M, Zatz M. Protein defects in neuromuscular diseases [Internet]. Brazilian Journal of Medical and Biological Research. 2003 ; 36 543-555.[citado 2024 jul. 09 ] Available from: https://doi.org/10.1590/S0100-879X2003000500001
  • 1

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