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Artigo de periodico
Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female (1996)
Toledo, S. P. A.; Bunner, H G; Kraaij, R; Post, M; Dahia, P L M; Hayashida, C Y; Kremer, H; Themmen, A P N
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 27 jul. 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 jul. 27 ]
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 jul. 27 ]
Trabalho de evento-resumo
Missense mutation in the lh receptor gene causas leydig cell hypoplasia (1995)
Themmen, A P N; Kraais, R; Kremer, H; Post, M; Toledo, S. P. A.; Brunner, H G; Grootegoed, J A
Fonte: Program and Abstracts. Nome do evento: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 27 jul. 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 jul. 27 ]
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 jul. 27 ]
Artigo de periodico
Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene (1995)
Kremer, H; Kraaij, R; Toledo, S. P. A.; Post, M; Fridman, J B; Hayashida, C Y; Reen, M; Milgrom, E.; Ropers, H H; Mariman, E; Themmen, A P N; Brunner, H G
Fonte: Nature Genetics. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 27 jul. 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 jul. 27 ] 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 jul. 27 ] Available from: https://doi.org/10.1038/ng0295-160

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