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Filtros : "Alonso, Luís G" Limpar

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  • Trabalho de evento-resumo periodico

    A mild form of autosomal recessive craniotubular dyplasia in a large inbred brazilian family (1999)

    Passos-Bueno, Maria Rita ; Wilcox, William R; Alonso, N.; Alonso, Luís G

    Source: American Journal of Human Genetics. Conference titles: 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

      PASSOS-BUENO, Maria Rita et al. A mild form of autosomal recessive craniotubular dyplasia in a large inbred brazilian family. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 27 abr. 2024. , 1999

    • APA

      Passos-Bueno, M. R., Wilcox, W. R., Alonso, N., & Alonso, L. G. (1999). A mild form of autosomal recessive craniotubular dyplasia in a large inbred brazilian family. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo.

    • NLM

      Passos-Bueno MR, Wilcox WR, Alonso N, Alonso LG. A mild form of autosomal recessive craniotubular dyplasia in a large inbred brazilian family. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2024 abr. 27 ]

    • Vancouver

      Passos-Bueno MR, Wilcox WR, Alonso N, Alonso LG. A mild form of autosomal recessive craniotubular dyplasia in a large inbred brazilian family. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2024 abr. 27 ]

  • Artigo de periodico

    Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses (1998)

    Passos-Bueno, Maria Rita ; Sertié, Andréa L; Richieri-Costa, Antonio; Alonso, Luís G; Zatz, Mayana ; Alonso, Nivaldo; Brunoni, Decio; Ribeiro, Sandra F M

    Source: American Journal of Medical Genetics. Unidades: IB, HRAC

    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. Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses. American Journal of Medical Genetics, v. 78, p. 237-241, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m. Acesso em: 27 abr. 2024.

    • APA

      Passos-Bueno, M. R., Sertié, A. L., Richieri-Costa, A., Alonso, L. G., Zatz, M., Alonso, N., et al. (1998). Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses. American Journal of Medical Genetics, 78, 237-241. doi:10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m

    • NLM

      Passos-Bueno MR, Sertié AL, Richieri-Costa A, Alonso LG, Zatz M, Alonso N, Brunoni D, Ribeiro SFM. Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses [Internet]. American Journal of Medical Genetics. 1998 ; 78 237-241.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m

    • Vancouver

      Passos-Bueno MR, Sertié AL, Richieri-Costa A, Alonso LG, Zatz M, Alonso N, Brunoni D, Ribeiro SFM. Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses [Internet]. American Journal of Medical Genetics. 1998 ; 78 237-241.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m
  • 1

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