Filtros : "Sumita, Denilce" Limpar

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  • Source: Genetics and Molecular Biology. Conference titles: Congresso Nacional de Genética. Unidade: IB

    Assunto: GENÉTICA

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

      MORAES, Lúcia et al. Parental origin and inactivation pattern of the extra X chromosomes in patients with 49, XXXXY and 49, XXXXX karyotypes. Genetics and Molecular Biology. Ribeirão Preto: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 13 out. 2024. , 1998
    • APA

      Moraes, L., Sumita, D., Zatz, M., Bastos, E., & Llerena, J. (1998). Parental origin and inactivation pattern of the extra X chromosomes in patients with 49, XXXXY and 49, XXXXX karyotypes. Genetics and Molecular Biology. Ribeirão Preto: Instituto de Biociências, Universidade de São Paulo.
    • NLM

      Moraes L, Sumita D, Zatz M, Bastos E, Llerena J. Parental origin and inactivation pattern of the extra X chromosomes in patients with 49, XXXXY and 49, XXXXX karyotypes. Genetics and Molecular Biology. 1998 ; 21( 3 suppl.): se 1998.[citado 2024 out. 13 ]
    • Vancouver

      Moraes L, Sumita D, Zatz M, Bastos E, Llerena J. Parental origin and inactivation pattern of the extra X chromosomes in patients with 49, XXXXY and 49, XXXXX karyotypes. Genetics and Molecular Biology. 1998 ; 21( 3 suppl.): se 1998.[citado 2024 out. 13 ]
  • Source: American Journal of Medical Genetics. 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

      ZATZ, Mayana et al. Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases. American Journal of Medical Genetics, v. 78, p. 361-365, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980724)78:4%3C361::aid-ajmg11%3E3.0.co;2-g. Acesso em: 13 out. 2024.
    • APA

      Zatz, M., Sumita, D., Campiotto, S., Canovas, M., Cerqueira, A., Vainzof, M., & Passos-Bueno, M. R. (1998). Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases. American Journal of Medical Genetics, 78, 361-365. doi:10.1002/(sici)1096-8628(19980724)78:4%3C361::aid-ajmg11%3E3.0.co;2-g
    • NLM

      Zatz M, Sumita D, Campiotto S, Canovas M, Cerqueira A, Vainzof M, Passos-Bueno MR. Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases [Internet]. American Journal of Medical Genetics. 1998 ; 78 361-365.[citado 2024 out. 13 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980724)78:4%3C361::aid-ajmg11%3E3.0.co;2-g
    • Vancouver

      Zatz M, Sumita D, Campiotto S, Canovas M, Cerqueira A, Vainzof M, Passos-Bueno MR. Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases [Internet]. American Journal of Medical Genetics. 1998 ; 78 361-365.[citado 2024 out. 13 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980724)78:4%3C361::aid-ajmg11%3E3.0.co;2-g

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