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Filtros : "Eng, C" Limpar

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  • Artigo de periodico

    Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas (1995)

    Eng, C; Crossey, P A; Mulligan, L M; Healey, C S; Houghton, C; Prowse, A; Chew, S L; Dahia, P L M; Oriordan, J L H; Toledo, S. P. A.; Smith, D P; Maher, E R

    Source: Journal of Medical Genetics. 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

      ENG, C et al. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas. Journal of Medical Genetics, v. 32, n. 12, p. 934-7, 1995Tradução . . Disponível em: https://doi.org/10.1136/jmg.32.12.934. Acesso em: 28 set. 2024.

    • APA

      Eng, C., Crossey, P. A., Mulligan, L. M., Healey, C. S., Houghton, C., Prowse, A., et al. (1995). Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas. Journal of Medical Genetics, 32( 12), 934-7. doi:10.1136/jmg.32.12.934

    • NLM

      Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PLM, Oriordan JLH, Toledo SPA, Smith DP, Maher ER. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas [Internet]. Journal of Medical Genetics. 1995 ;32( 12): 934-7.[citado 2024 set. 28 ] Available from: https://doi.org/10.1136/jmg.32.12.934

    • Vancouver

      Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PLM, Oriordan JLH, Toledo SPA, Smith DP, Maher ER. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas [Internet]. Journal of Medical Genetics. 1995 ;32( 12): 934-7.[citado 2024 set. 28 ] Available from: https://doi.org/10.1136/jmg.32.12.934

  • Trabalho de evento-resumo

    Molecular analysis of p53 vhl and ret genes in pheochromocytoma (1995)

    Dahia, P L M; Aguiar, R C T; Eng, C; Crossey, P A; Maher, E R; Grossman, A; Ponder, B A J; Toledo, S. P. A.

    Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM

    Assunto: ENDOCRINOLOGIA

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

    • ABNT

      DAHIA, P L M et al. Molecular analysis of p53 vhl and ret genes in pheochromocytoma. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 28 set. 2024.

    • APA

      Dahia, P. L. M., Aguiar, R. C. T., Eng, C., Crossey, P. A., Maher, E. R., Grossman, A., et al. (1995). Molecular analysis of p53 vhl and ret genes in pheochromocytoma. In Program and Abstracts. Rockville: Endocrine Society.

    • NLM

      Dahia PLM, Aguiar RCT, Eng C, Crossey PA, Maher ER, Grossman A, Ponder BAJ, Toledo SPA. Molecular analysis of p53 vhl and ret genes in pheochromocytoma. Program and Abstracts. 1995 ;[citado 2024 set. 28 ]

    • Vancouver

      Dahia PLM, Aguiar RCT, Eng C, Crossey PA, Maher ER, Grossman A, Ponder BAJ, Toledo SPA. Molecular analysis of p53 vhl and ret genes in pheochromocytoma. Program and Abstracts. 1995 ;[citado 2024 set. 28 ]

  • Artigo de periodico

    Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours (1994)

    Eng, C; Smith, D P; Mulligan, L M; Nagai, Maria Aparecida; Healey, C S; Ponder, M A; Gardner, E; Schelimann, G F W; Jackson, C E; Tunnacliffe, A; Ponder, B A J

    Source: Human Molecular Genetics. Unidade: FM

    Assunto: ONCOLOGIA

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

    • ABNT

      ENG, C et al. Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours. Human Molecular Genetics, v. 3 , n. 2 , p. 237-41, 1994Tradução . . Disponível em: https://doi.org/10.1093/hmg/3.2.237. Acesso em: 28 set. 2024.

    • APA

      Eng, C., Smith, D. P., Mulligan, L. M., Nagai, M. A., Healey, C. S., Ponder, M. A., et al. (1994). Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours. Human Molecular Genetics, 3 ( 2 ), 237-41. doi:10.1093/hmg/3.2.237

    • NLM

      Eng C, Smith DP, Mulligan LM, Nagai MA, Healey CS, Ponder MA, Gardner E, Schelimann GFW, Jackson CE, Tunnacliffe A, Ponder BAJ. Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours [Internet]. Human Molecular Genetics. 1994 ;3 ( 2 ): 237-41.[citado 2024 set. 28 ] Available from: https://doi.org/10.1093/hmg/3.2.237

    • Vancouver

      Eng C, Smith DP, Mulligan LM, Nagai MA, Healey CS, Ponder MA, Gardner E, Schelimann GFW, Jackson CE, Tunnacliffe A, Ponder BAJ. Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours [Internet]. Human Molecular Genetics. 1994 ;3 ( 2 ): 237-41.[citado 2024 set. 28 ] Available from: https://doi.org/10.1093/hmg/3.2.237
  • 1

1 - 3 (3 records)

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