Filtros : "Indexado no Biological Abstracts" "DNA" "FORP" Removidos: "Odontologia Legal" "FMRP-RCM" "1993" "Financiamento DECIT" Limpar

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  • Source: Clinica Chimica Acta. Unidades: FMRP, FORP

    Subjects: TROMBOEMBOLISMO, PLASMA, DNA

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

      UZUELLI, Juliana A. et al. Circulating cell-free DNA levels in plasma increase with severity in experimental acute pulmonary thromboembolism. Clinica Chimica Acta, v. 409, n. 1-2, p. 112-116, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.cca.2009.09.011. Acesso em: 04 out. 2024.
    • APA

      Uzuelli, J. A., Dias-Júnior, C. A. C., Izidoro-Toledo, T. C., Gerlach, R. F., & Tanus-Santos, J. E. (2009). Circulating cell-free DNA levels in plasma increase with severity in experimental acute pulmonary thromboembolism. Clinica Chimica Acta, 409( 1-2), 112-116. doi:10.1016/j.cca.2009.09.011
    • NLM

      Uzuelli JA, Dias-Júnior CAC, Izidoro-Toledo TC, Gerlach RF, Tanus-Santos JE. Circulating cell-free DNA levels in plasma increase with severity in experimental acute pulmonary thromboembolism [Internet]. Clinica Chimica Acta. 2009 ; 409( 1-2): 112-116.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.cca.2009.09.011
    • Vancouver

      Uzuelli JA, Dias-Júnior CAC, Izidoro-Toledo TC, Gerlach RF, Tanus-Santos JE. Circulating cell-free DNA levels in plasma increase with severity in experimental acute pulmonary thromboembolism [Internet]. Clinica Chimica Acta. 2009 ; 409( 1-2): 112-116.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.cca.2009.09.011
  • Source: Mutagenesis. Unidades: FORP, FFCLRP

    Subjects: DNA, ONCOGENES

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

      PEITL, Paulo et al. Chromosomal rearrangements involving telomeric DNA sequences in Balb/3T3 cells transfected with the Ha-ras oncogene. Mutagenesis, v. 17, n. 1, p. 67-72, 2002Tradução . . Disponível em: https://doi.org/10.1093/mutage/17.1.67. Acesso em: 04 out. 2024.
    • APA

      Peitl, P., Mello, S. S., Camparoto, M. L., Passos, G. A. S., Hande, M. P., Cardoso, R. S., & Sakamoto-Hojo, E. T. (2002). Chromosomal rearrangements involving telomeric DNA sequences in Balb/3T3 cells transfected with the Ha-ras oncogene. Mutagenesis, 17( 1), 67-72. doi:10.1093/mutage/17.1.67
    • NLM

      Peitl P, Mello SS, Camparoto ML, Passos GAS, Hande MP, Cardoso RS, Sakamoto-Hojo ET. Chromosomal rearrangements involving telomeric DNA sequences in Balb/3T3 cells transfected with the Ha-ras oncogene [Internet]. Mutagenesis. 2002 ; 17( 1): 67-72.[citado 2024 out. 04 ] Available from: https://doi.org/10.1093/mutage/17.1.67
    • Vancouver

      Peitl P, Mello SS, Camparoto ML, Passos GAS, Hande MP, Cardoso RS, Sakamoto-Hojo ET. Chromosomal rearrangements involving telomeric DNA sequences in Balb/3T3 cells transfected with the Ha-ras oncogene [Internet]. Mutagenesis. 2002 ; 17( 1): 67-72.[citado 2024 out. 04 ] Available from: https://doi.org/10.1093/mutage/17.1.67
  • Source: Clinical genetics. Unidades: FMRP, HRAC, FORP

    Subjects: GENÉTICA, DNA

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

      SANDRIN GARCIA, P et al. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome. Clinical genetics, v. 61, n. 5, p. 380-383, 2002Tradução . . Disponível em: https://doi.org/10.1034/j.1399-0004.2002.610511.x. Acesso em: 04 out. 2024.
    • APA

      Sandrin Garcia, P., Macedo, C., Martelli, L. R., Ramos, E. S., Guion Almeida, M. L., Richieri Costa, A., & Passos, G. A. S. (2002). Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome. Clinical genetics, 61( 5), 380-383. doi:10.1034/j.1399-0004.2002.610511.x
    • NLM

      Sandrin Garcia P, Macedo C, Martelli LR, Ramos ES, Guion Almeida ML, Richieri Costa A, Passos GAS. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome [Internet]. Clinical genetics. 2002 ; 61( 5): 380-383.[citado 2024 out. 04 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x
    • Vancouver

      Sandrin Garcia P, Macedo C, Martelli LR, Ramos ES, Guion Almeida ML, Richieri Costa A, Passos GAS. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome [Internet]. Clinical genetics. 2002 ; 61( 5): 380-383.[citado 2024 out. 04 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x

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