Filtros : "Rodrigues, Tatiane C." Limpar

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  • Source: European Journal of Endocrinology. Unidades: IB, FM

    Subjects: GENES, IDADE GESTACIONAL, CRESCIMENTO E DESENVOLVIMENTO

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

      CANTON, Ana P. M. et al. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways. European Journal of Endocrinology, v. 171, n. 2, p. 253-262, 2014Tradução . . Disponível em: https://doi.org/10.1530/eje-14-0232. Acesso em: 21 maio 2024.
    • APA

      Canton, A. P. M., Costa, S. S., Rodrigues, T. C., Bertola, D. R., Malaquias, A. C., Correa, F. A., et al. (2014). Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways. European Journal of Endocrinology, 171( 2), 253-262. doi:10.1530/eje-14-0232
    • NLM

      Canton APM, Costa SS, Rodrigues TC, Bertola DR, Malaquias AC, Correa FA, Arnhold IJP, Rosenberg C, Jorge AAL. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways [Internet]. European Journal of Endocrinology. 2014 ; 171( 2): 253-262.[citado 2024 maio 21 ] Available from: https://doi.org/10.1530/eje-14-0232
    • Vancouver

      Canton APM, Costa SS, Rodrigues TC, Bertola DR, Malaquias AC, Correa FA, Arnhold IJP, Rosenberg C, Jorge AAL. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways [Internet]. European Journal of Endocrinology. 2014 ; 171( 2): 253-262.[citado 2024 maio 21 ] Available from: https://doi.org/10.1530/eje-14-0232
  • Source: Meta Gene. Unidade: IB

    Subjects: ANOMALIA DENTÁRIA, GENES

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

      LINHARES, Natália D. et al. Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene. Meta Gene, v. 2, p. 16-24, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.mgene.2013.10.005. Acesso em: 21 maio 2024.
    • APA

      Linhares, N. D., Svartman, M., Salgado, M. I., Rodrigues, T. C., Costa, S. S. da, Rosenberg, C., & Valadares, E. R. (2014). Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene. Meta Gene, 2, 16-24. doi:10.1016/j.mgene.2013.10.005
    • NLM

      Linhares ND, Svartman M, Salgado MI, Rodrigues TC, Costa SS da, Rosenberg C, Valadares ER. Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene [Internet]. Meta Gene. 2014 ; 2 16-24.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.mgene.2013.10.005
    • Vancouver

      Linhares ND, Svartman M, Salgado MI, Rodrigues TC, Costa SS da, Rosenberg C, Valadares ER. Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene [Internet]. Meta Gene. 2014 ; 2 16-24.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.mgene.2013.10.005

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