Missense mutation in the lh receptor gene causas leydig cell hypoplasia (1995)
- Autores:
- Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Idioma: Inglês
- Imprenta:
- Editora: Endocrine Society
- Local: Rockville
- Data de publicação: 1995
- Fonte:
- Título do periódico: Program and Abstracts
- Nome do evento: Annual Meeting of the Endocrine Society
-
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 ] - Carcinoma medular de tireoide
- Sindrome hereditaria caracterizada por micropenis, hipoandrogenismo e niveis sericos altos de gonadotrofinas devido a disturbio primario nas celulas de leydig, associada a testiculos de tamanho normal e ausencia de ambiguidade genital: uma provavel nova entidade clinica
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