Filtros : "Post, M" Limpar

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

    Assunto: ENDOCRINOLOGIA

    How to cite
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    • ABNT

      TOLEDO, S. P. A. et al. Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female. Journal of Clinical Endocrinology and Metabolism, v. no 1996, n. 11, p. 3850-4, 1996Tradução . . Acesso em: 15 jun. 2024.
    • APA

      Toledo, S. P. A., Bunner, H. G., Kraaij, R., Post, M., Dahia, P. L. M., Hayashida, C. Y., et al. (1996). Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female. Journal of Clinical Endocrinology and Metabolism, no 1996( 11), 3850-4.
    • NLM

      Toledo SPA, Bunner HG, Kraaij R, Post M, Dahia PLM, Hayashida CY, Kremer H, Themmen APN. Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female. Journal of Clinical Endocrinology and Metabolism. 1996 ; no 1996( 11): 3850-4.[citado 2024 jun. 15 ]
    • Vancouver

      Toledo SPA, Bunner HG, Kraaij R, Post M, Dahia PLM, Hayashida CY, Kremer H, Themmen APN. Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female. Journal of Clinical Endocrinology and Metabolism. 1996 ; no 1996( 11): 3850-4.[citado 2024 jun. 15 ]
  • Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM

    Assunto: ENDOCRINOLOGIA

    How to cite
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    • ABNT

      THEMMEN, A P N et al. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 15 jun. 2024.
    • APA

      Themmen, A. P. N., Kraais, R., Kremer, H., Post, M., Toledo, S. P. A., Brunner, H. G., & Grootegoed, J. A. (1995). Missense mutation in the lh receptor gene causas leydig cell hypoplasia. In Program and Abstracts. Rockville: Endocrine Society.
    • NLM

      Themmen APN, Kraais R, Kremer H, Post M, Toledo SPA, Brunner HG, Grootegoed JA. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. Program and Abstracts. 1995 ;[citado 2024 jun. 15 ]
    • Vancouver

      Themmen APN, Kraais R, Kremer H, Post M, Toledo SPA, Brunner HG, Grootegoed JA. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. Program and Abstracts. 1995 ;[citado 2024 jun. 15 ]
  • Source: Nature Genetics. Unidade: FM

    Assunto: ENDOCRINOLOGIA

    Acesso à fonteDOIHow to cite
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    • ABNT

      KREMER, H et al. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene. Nature Genetics, v. 9 , p. 160-4, 1995Tradução . . Disponível em: https://doi.org/10.1038/ng0295-160. Acesso em: 15 jun. 2024.
    • APA

      Kremer, H., Kraaij, R., Toledo, S. P. A., Post, M., Fridman, J. B., Hayashida, C. Y., et al. (1995). Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene. Nature Genetics, 9 , 160-4. doi:10.1038/ng0295-160
    • NLM

      Kremer H, Kraaij R, Toledo SPA, Post M, Fridman JB, Hayashida CY, Reen M, Milgrom E, Ropers HH, Mariman E, Themmen APN, Brunner HG. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene [Internet]. Nature Genetics. 1995 ;9 160-4.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1038/ng0295-160
    • Vancouver

      Kremer H, Kraaij R, Toledo SPA, Post M, Fridman JB, Hayashida CY, Reen M, Milgrom E, Ropers HH, Mariman E, Themmen APN, Brunner HG. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene [Internet]. Nature Genetics. 1995 ;9 160-4.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1038/ng0295-160

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