Filtros : "CITOGENÉTICA" "Chauffaille, Maria de Lourdes" Removidos: "Fissuras Orofaciais e Anomalias Relacionadas" "Tone, Luiz Gonzaga" "2000" Limpar

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  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: CITOGENÉTICA, LEUCEMIA MIELOIDE AGUDA, POLIMORFISMO, ANÁLISE SEQUENCIAL, DNA

    PrivadoAcesso à fonteAcesso à fonteDOIHow to cite
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    • ABNT

      NORONHA, Thiago Rodrigo de e MITNE-NETO, Miguel e CHAUFFAILLE, Maria de Lourdes. JAK2-mutated acute myeloid leukemia: comparison of next-generation sequencing (NGS) and single nucleotide polymorphism array (SNPa) findings between two cases. Autopsy and Case Reports, v. 9, n. apr./ju 2019, p. e2018084, 2019Tradução . . Disponível em: https://doi.org/10.4322/acr.2018.084. Acesso em: 29 jun. 2024.
    • APA

      Noronha, T. R. de, Mitne-Neto, M., & Chauffaille, M. de L. (2019). JAK2-mutated acute myeloid leukemia: comparison of next-generation sequencing (NGS) and single nucleotide polymorphism array (SNPa) findings between two cases. Autopsy and Case Reports, 9( apr./ju 2019), e2018084. doi:10.4322/acr.2018.084
    • NLM

      Noronha TR de, Mitne-Neto M, Chauffaille M de L. JAK2-mutated acute myeloid leukemia: comparison of next-generation sequencing (NGS) and single nucleotide polymorphism array (SNPa) findings between two cases [Internet]. Autopsy and Case Reports. 2019 ; 9( apr./ju 2019): e2018084.[citado 2024 jun. 29 ] Available from: https://doi.org/10.4322/acr.2018.084
    • Vancouver

      Noronha TR de, Mitne-Neto M, Chauffaille M de L. JAK2-mutated acute myeloid leukemia: comparison of next-generation sequencing (NGS) and single nucleotide polymorphism array (SNPa) findings between two cases [Internet]. Autopsy and Case Reports. 2019 ; 9( apr./ju 2019): e2018084.[citado 2024 jun. 29 ] Available from: https://doi.org/10.4322/acr.2018.084
  • Source: Journal of Investigative Medicine. Unidade: HU

    Subjects: LEUCEMIA MIELOIDE AGUDA, CITOGENÉTICA, POLIMORFISMO, SEQUENCIAMENTO GENÉTICO

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

      NORONHA, Thiago Rodrigo de e MITNE-NETO, Miguel e CHAUFFAILLE, Maria de Lourdes. Mutational profiling of acute myeloid leukemia with normal cytogenetics in Brazilian patients: the value of next-generation sequencing for genomic classification. Journal of Investigative Medicine, v. 65, n. 8, p. 1155-1158, 2017Tradução . . Disponível em: https://doi.org/10.1136/jim-2017-000566. Acesso em: 29 jun. 2024.
    • APA

      Noronha, T. R. de, Mitne-Neto, M., & Chauffaille, M. de L. (2017). Mutational profiling of acute myeloid leukemia with normal cytogenetics in Brazilian patients: the value of next-generation sequencing for genomic classification. Journal of Investigative Medicine, 65( 8), 1155-1158. doi:10.1136/jim-2017-000566
    • NLM

      Noronha TR de, Mitne-Neto M, Chauffaille M de L. Mutational profiling of acute myeloid leukemia with normal cytogenetics in Brazilian patients: the value of next-generation sequencing for genomic classification [Internet]. Journal of Investigative Medicine. 2017 ; 65( 8): 1155-1158.[citado 2024 jun. 29 ] Available from: https://doi.org/10.1136/jim-2017-000566
    • Vancouver

      Noronha TR de, Mitne-Neto M, Chauffaille M de L. Mutational profiling of acute myeloid leukemia with normal cytogenetics in Brazilian patients: the value of next-generation sequencing for genomic classification [Internet]. Journal of Investigative Medicine. 2017 ; 65( 8): 1155-1158.[citado 2024 jun. 29 ] Available from: https://doi.org/10.1136/jim-2017-000566
  • Source: Medical Oncology. Unidade: FMRP

    Subjects: LEUCEMIA MIELOIDE AGUDA, CITOGENÉTICA

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

      LUCENA-ARAUJO, Antonio Roberto et al. Identification of a new translocation that disrupts the RUNX1 gene in a patient with de novo acute myeloid leukemia. Medical Oncology, v. 29, n. 2, p. 1114-1118, 2012Tradução . . Disponível em: https://doi.org/10.1007/s12032-011-9890-3. Acesso em: 29 jun. 2024.
    • APA

      Lucena-Araujo, A. R., Figueiredo-Pontes, L. L., Oliveira, F. M. de, Chauffaille, M. de L., Falcao, R. P., & Rego, E. M. (2012). Identification of a new translocation that disrupts the RUNX1 gene in a patient with de novo acute myeloid leukemia. Medical Oncology, 29( 2), 1114-1118. doi:10.1007/s12032-011-9890-3
    • NLM

      Lucena-Araujo AR, Figueiredo-Pontes LL, Oliveira FM de, Chauffaille M de L, Falcao RP, Rego EM. Identification of a new translocation that disrupts the RUNX1 gene in a patient with de novo acute myeloid leukemia [Internet]. Medical Oncology. 2012 ; 29( 2): 1114-1118.[citado 2024 jun. 29 ] Available from: https://doi.org/10.1007/s12032-011-9890-3
    • Vancouver

      Lucena-Araujo AR, Figueiredo-Pontes LL, Oliveira FM de, Chauffaille M de L, Falcao RP, Rego EM. Identification of a new translocation that disrupts the RUNX1 gene in a patient with de novo acute myeloid leukemia [Internet]. Medical Oncology. 2012 ; 29( 2): 1114-1118.[citado 2024 jun. 29 ] Available from: https://doi.org/10.1007/s12032-011-9890-3

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