Filtros : "Byth, B C" Limpar

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  • Source: American Journal of Medical Genetics. Unidades: FM, 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

      PASSOS-BUENO, Maria Rita et al. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation?. American Journal of Medical Genetics, v. 46, n. 2 , p. 172-5, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460214. Acesso em: 10 jun. 2024.
    • APA

      Passos-Bueno, M. R., Byth, B. C., Rosemberg, S., Takata, R. I., Bakker, E., Beggs, A. H., et al. (1993). Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? American Journal of Medical Genetics, 46( 2 ), 172-5. doi:10.1002/ajmg.1320460214
    • NLM

      Passos-Bueno MR, Byth BC, Rosemberg S, Takata RI, Bakker E, Beggs AH, Pavanello RCM, Vainzof M, Davies KE, Zatz M. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? [Internet]. American Journal of Medical Genetics. 1993 ;46( 2 ): 172-5.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1002/ajmg.1320460214
    • Vancouver

      Passos-Bueno MR, Byth BC, Rosemberg S, Takata RI, Bakker E, Beggs AH, Pavanello RCM, Vainzof M, Davies KE, Zatz M. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? [Internet]. American Journal of Medical Genetics. 1993 ;46( 2 ): 172-5.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1002/ajmg.1320460214
  • Source: Nucleic Acids Research. Unidade: IB

    Assunto: GENÉTICA MÉDICA

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

      BYTH, B C et al. New dna marker, d6s129, identifies a hindiii polymorphism on chromosome 6q. Nucleic Acids Research, v. 19, n. 15, p. 4310, 1991Tradução . . Acesso em: 10 jun. 2024.
    • APA

      Byth, B. C., Love, D. R., Passos-Bueno, M. R., & Davies, K. E. (1991). New dna marker, d6s129, identifies a hindiii polymorphism on chromosome 6q. Nucleic Acids Research, 19( 15), 4310.
    • NLM

      Byth BC, Love DR, Passos-Bueno MR, Davies KE. New dna marker, d6s129, identifies a hindiii polymorphism on chromosome 6q. Nucleic Acids Research. 1991 ;19( 15): 4310.[citado 2024 jun. 10 ]
    • Vancouver

      Byth BC, Love DR, Passos-Bueno MR, Davies KE. New dna marker, d6s129, identifies a hindiii polymorphism on chromosome 6q. Nucleic Acids Research. 1991 ;19( 15): 4310.[citado 2024 jun. 10 ]

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