Filtros : "Medeiros Neto, Geraldo Antônio" "Varela, V" "FM" Removidos: "IP-PST" "NORONHA, IRENE DE LOURDES" "1930" "EDITOR DE PERIODICO" Limpar

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  • Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM

    Assunto: ENDOCRINOLOGIA

    Acesso à fonteDOIHow to cite
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    • ABNT

      TARGOVNIK, H M et al. 138- nucleotid deletion in the thyroglobulin ribunocleic acid messenger in a congenital goiter with defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism, v. no 1995, n. 11, p. 3356-60, 1995Tradução . . Disponível em: https://doi.org/10.1210/jcem.80.11.7593451. Acesso em: 29 jul. 2024.
    • APA

      Targovnik, H. M., Vono, J., Billerbeck, A. E. C., Cerrone, G. E., Varela, V., Mendive, F., et al. (1995). 138- nucleotid deletion in the thyroglobulin ribunocleic acid messenger in a congenital goiter with defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism, no 1995( 11), 3356-60. doi:10.1210/jcem.80.11.7593451
    • NLM

      Targovnik HM, Vono J, Billerbeck AEC, Cerrone GE, Varela V, Mendive F, Wajchenberg BL, Medeiros Neto GA. 138- nucleotid deletion in the thyroglobulin ribunocleic acid messenger in a congenital goiter with defective thyroglobulin synthesis [Internet]. Journal of Clinical Endocrinology and Metabolism. 1995 ; no 1995( 11): 3356-60.[citado 2024 jul. 29 ] Available from: https://doi.org/10.1210/jcem.80.11.7593451
    • Vancouver

      Targovnik HM, Vono J, Billerbeck AEC, Cerrone GE, Varela V, Mendive F, Wajchenberg BL, Medeiros Neto GA. 138- nucleotid deletion in the thyroglobulin ribunocleic acid messenger in a congenital goiter with defective thyroglobulin synthesis [Internet]. Journal of Clinical Endocrinology and Metabolism. 1995 ; no 1995( 11): 3356-60.[citado 2024 jul. 29 ] Available from: https://doi.org/10.1210/jcem.80.11.7593451
  • Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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

      TARGOVNIK, H M et al. Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger. Journal of Clinical Endocrinology and Metabolism, v. 77, n. 1 , p. 210-5, 1993Tradução . . Disponível em: https://doi.org/10.1210/jcem.77.1.8325944. Acesso em: 29 jul. 2024.
    • APA

      Targovnik, H. M., Medeiros Neto, G. A., Varela, V., Cochaux, P., Wajchenberg, B. L., & Vassart, G. (1993). Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger. Journal of Clinical Endocrinology and Metabolism, 77( 1 ), 210-5. doi:10.1210/jcem.77.1.8325944
    • NLM

      Targovnik HM, Medeiros Neto GA, Varela V, Cochaux P, Wajchenberg BL, Vassart G. Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger [Internet]. Journal of Clinical Endocrinology and Metabolism. 1993 ;77( 1 ): 210-5.[citado 2024 jul. 29 ] Available from: https://doi.org/10.1210/jcem.77.1.8325944
    • Vancouver

      Targovnik HM, Medeiros Neto GA, Varela V, Cochaux P, Wajchenberg BL, Vassart G. Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger [Internet]. Journal of Clinical Endocrinology and Metabolism. 1993 ;77( 1 ): 210-5.[citado 2024 jul. 29 ] Available from: https://doi.org/10.1210/jcem.77.1.8325944
  • Source: Journal of Endocrinological Investigation. Unidade: FM

    Assunto: ENDOCRINOLOGIA

    Acesso à fonteDOIHow to cite
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    • ABNT

      TARGOVNIK, H M et al. Human thyroid tissue do not express thyroalbumin. Journal of Endocrinological Investigation, v. 16, p. 415-9, 1993Tradução . . Disponível em: https://doi.org/10.1007/bf03348869. Acesso em: 29 jul. 2024.
    • APA

      Targovnik, H. M., Frechtel, G. D., Varela, V., Wajchenberg, B. L., Vassart, G., Dumont, J., & Medeiros Neto, G. A. (1993). Human thyroid tissue do not express thyroalbumin. Journal of Endocrinological Investigation, 16, 415-9. doi:10.1007/bf03348869
    • NLM

      Targovnik HM, Frechtel GD, Varela V, Wajchenberg BL, Vassart G, Dumont J, Medeiros Neto GA. Human thyroid tissue do not express thyroalbumin [Internet]. Journal of Endocrinological Investigation. 1993 ;16 415-9.[citado 2024 jul. 29 ] Available from: https://doi.org/10.1007/bf03348869
    • Vancouver

      Targovnik HM, Frechtel GD, Varela V, Wajchenberg BL, Vassart G, Dumont J, Medeiros Neto GA. Human thyroid tissue do not express thyroalbumin [Internet]. Journal of Endocrinological Investigation. 1993 ;16 415-9.[citado 2024 jul. 29 ] Available from: https://doi.org/10.1007/bf03348869
  • Source: Journal of Endocrinological Investigation. Conference titles: Annual Meeting of the European Thyroid Association. Unidade: FM

    Assunto: ENDOCRINOLOGIA

    How to cite
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    • ABNT

      TARGOVNIK, H M et al. Nonsense mutation with preferential production of a 171 nt deleted tg 'ANTIND.M RNA' as cause of human congenital goiter. Journal of Endocrinological Investigation. Milano: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 29 jul. 2024. , 1992
    • APA

      Targovnik, H. M., Varela, V., Cochaux, P., & Medeiros Neto, G. A. (1992). Nonsense mutation with preferential production of a 171 nt deleted tg 'ANTIND.M RNA' as cause of human congenital goiter. Journal of Endocrinological Investigation. Milano: Faculdade de Medicina, Universidade de São Paulo.
    • NLM

      Targovnik HM, Varela V, Cochaux P, Medeiros Neto GA. Nonsense mutation with preferential production of a 171 nt deleted tg 'ANTIND.M RNA' as cause of human congenital goiter. Journal of Endocrinological Investigation. 1992 ;15( 5 suppl.2): 39.[citado 2024 jul. 29 ]
    • Vancouver

      Targovnik HM, Varela V, Cochaux P, Medeiros Neto GA. Nonsense mutation with preferential production of a 171 nt deleted tg 'ANTIND.M RNA' as cause of human congenital goiter. Journal of Endocrinological Investigation. 1992 ;15( 5 suppl.2): 39.[citado 2024 jul. 29 ]
  • Source: Thyroid. Unidade: FM

    Assunto: ENDOCRINOLOGIA

    How to cite
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    • ABNT

      TARGOVNIK, H M et al. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis. Thyroid, v. 1 , n. 4 , p. 339-45, 1991Tradução . . Acesso em: 29 jul. 2024.
    • APA

      Targovnik, H. M., Varela, V., Abatangelo, C., Wajchenberg, B. L., & Medeiros Neto, G. A. (1991). Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis. Thyroid, 1 ( 4 ), 339-45.
    • NLM

      Targovnik HM, Varela V, Abatangelo C, Wajchenberg BL, Medeiros Neto GA. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis. Thyroid. 1991 ;1 ( 4 ): 339-45.[citado 2024 jul. 29 ]
    • Vancouver

      Targovnik HM, Varela V, Abatangelo C, Wajchenberg BL, Medeiros Neto GA. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis. Thyroid. 1991 ;1 ( 4 ): 339-45.[citado 2024 jul. 29 ]
  • Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM

    Assunto: ENDOCRINOLOGIA

    How to cite
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    • ABNT

      TARGOVNIK, H M et al. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin. 1991, Anais.. Washington: Endocrine Society, 1991. . Acesso em: 29 jul. 2024.
    • APA

      Targovnik, H. M., Varela, V., Abatangelo, C., Wajchenberg, B. L., & Medeiros Neto, G. A. (1991). Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin. In Program and Abstracts. Washington: Endocrine Society.
    • NLM

      Targovnik HM, Varela V, Abatangelo C, Wajchenberg BL, Medeiros Neto GA. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin. Program and Abstracts. 1991 ;[citado 2024 jul. 29 ]
    • Vancouver

      Targovnik HM, Varela V, Abatangelo C, Wajchenberg BL, Medeiros Neto GA. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin. Program and Abstracts. 1991 ;[citado 2024 jul. 29 ]
  • Source: Journal of Endocrinological Investigation. Unidade: FM

    Subjects: GLOBULINAS, BÓCIO, SEQUENCIAMENTO GENÉTICO

    Acesso à fonteDOIHow to cite
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    • ABNT

      MEDEIROS NETO, Geraldo Antônio et al. Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter . Absence of gross gene deletion of coding sequences in the tg gene structure. Journal of Endocrinological Investigation, v. 12, p. 805-13, 1989Tradução . . Disponível em: https://doi.org/10.1007/bf03350067. Acesso em: 29 jul. 2024.
    • APA

      Medeiros Neto, G. A., Targovnik, H., Knobel, M., Propato, F., Varela, V., Alkmin, M., et al. (1989). Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter . Absence of gross gene deletion of coding sequences in the tg gene structure. Journal of Endocrinological Investigation, 12, 805-13. doi:10.1007/bf03350067
    • NLM

      Medeiros Neto GA, Targovnik H, Knobel M, Propato F, Varela V, Alkmin M, Barbosa S, Wajchenberg BL. Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter . Absence of gross gene deletion of coding sequences in the tg gene structure [Internet]. Journal of Endocrinological Investigation. 1989 ;12 805-13.[citado 2024 jul. 29 ] Available from: https://doi.org/10.1007/bf03350067
    • Vancouver

      Medeiros Neto GA, Targovnik H, Knobel M, Propato F, Varela V, Alkmin M, Barbosa S, Wajchenberg BL. Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter . Absence of gross gene deletion of coding sequences in the tg gene structure [Internet]. Journal of Endocrinological Investigation. 1989 ;12 805-13.[citado 2024 jul. 29 ] Available from: https://doi.org/10.1007/bf03350067

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