Filtros : "Sexual development" Limpar

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  • Source: Sexual development. Unidade: FM

    Subjects: NEOPLASIAS RENAIS, GENES SUPRESSORES DE TUMOR

    Acesso à fonteDOIHow to cite
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    • ABNT

      FERRARI, M. T. M et al. WT1 pathogenic variants are associated with a broad spectrum of differences in sex development phenotypes and heterogeneous progression of renal disease. Sexual development, v. 16, n. 1, p. 46-54, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/58605. Acesso em: 28 jan. 2026.
    • APA

      Ferrari, M. T. M., Watanabe, A., Silva, T. E. D., Gomes, N. L., Batista, R. L., Nishi, M. Y., et al. (2023). WT1 pathogenic variants are associated with a broad spectrum of differences in sex development phenotypes and heterogeneous progression of renal disease. Sexual development, 16( 1), 46-54. doi:10.1159/000517373
    • NLM

      Ferrari MTM, Watanabe A, Silva TED, Gomes NL, Batista RL, Nishi MY, Paula LCPD, COSTA EC, Onuchic LF, Mendonca BB de. WT1 pathogenic variants are associated with a broad spectrum of differences in sex development phenotypes and heterogeneous progression of renal disease [Internet]. Sexual development. 2023 ; 16( 1): 46-54.[citado 2026 jan. 28 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58605
    • Vancouver

      Ferrari MTM, Watanabe A, Silva TED, Gomes NL, Batista RL, Nishi MY, Paula LCPD, COSTA EC, Onuchic LF, Mendonca BB de. WT1 pathogenic variants are associated with a broad spectrum of differences in sex development phenotypes and heterogeneous progression of renal disease [Internet]. Sexual development. 2023 ; 16( 1): 46-54.[citado 2026 jan. 28 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58605
  • Source: Sexual development. Unidade: FM

    Subjects: MUTAÇÃO GENÉTICA, FATORES DE RISCO, NEOPLASIAS DOS GENITAIS MASCULINOS

    Acesso à fonteDOIHow to cite
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    • ABNT

      BATISTA, Rafael Loch e MENDONCA, Berenice Bilharinho de. The Molecular Basis of 5 alpha-Reductase Type 2 Deficiency. Sexual development, v. 16, n. 2-3, p. 171-183, 2022Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/50394. Acesso em: 28 jan. 2026.
    • APA

      Batista, R. L., & Mendonca, B. B. de. (2022). The Molecular Basis of 5 alpha-Reductase Type 2 Deficiency. Sexual development, 16( 2-3), 171-183. doi:10.1159/000525119
    • NLM

      Batista RL, Mendonca BB de. The Molecular Basis of 5 alpha-Reductase Type 2 Deficiency [Internet]. Sexual development. 2022 ; 16( 2-3): 171-183.[citado 2026 jan. 28 ] Available from: https://observatorio.fm.usp.br/handle/OPI/50394
    • Vancouver

      Batista RL, Mendonca BB de. The Molecular Basis of 5 alpha-Reductase Type 2 Deficiency [Internet]. Sexual development. 2022 ; 16( 2-3): 171-183.[citado 2026 jan. 28 ] Available from: https://observatorio.fm.usp.br/handle/OPI/50394
  • Source: Sexual development. Unidade: FM

    Subjects: DOENÇAS GENÉTICAS, HOMENS, DESENVOLVIMENTO SEXUAL

    Acesso à fonteDOIHow to cite
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    • ABNT

      AHMED, S. Faisal et al. The Use of Genetics for Reaching a Diagnosis in XY DSD. Sexual development, v. 16, n. 2-3, p. 207-224, 2022Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/50425. Acesso em: 28 jan. 2026.
    • APA

      Ahmed, S. F., Alimusina, M., Batista, R. L., Domenice, S., Gomes, N. L., Mcgowan, R., et al. (2022). The Use of Genetics for Reaching a Diagnosis in XY DSD. Sexual development, 16( 2-3), 207-224. doi:10.1159/000524881
    • NLM

      Ahmed SF, Alimusina M, Batista RL, Domenice S, Gomes NL, Mcgowan R, Patjamontri S, Mendonca BB de. The Use of Genetics for Reaching a Diagnosis in XY DSD [Internet]. Sexual development. 2022 ; 16( 2-3): 207-224.[citado 2026 jan. 28 ] Available from: https://observatorio.fm.usp.br/handle/OPI/50425
    • Vancouver

      Ahmed SF, Alimusina M, Batista RL, Domenice S, Gomes NL, Mcgowan R, Patjamontri S, Mendonca BB de. The Use of Genetics for Reaching a Diagnosis in XY DSD [Internet]. Sexual development. 2022 ; 16( 2-3): 207-224.[citado 2026 jan. 28 ] Available from: https://observatorio.fm.usp.br/handle/OPI/50425

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