Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene (1998)
- Authors:
- Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Springfield
- Date published: 1998
- Source:
- Título do periódico: Journal of Clinical Endocrinology and Metabolism
- Volume/Número/Paginação/Ano: v. 84, n. 3, p. 917-923, 1998
-
ABNT
SALVATORI, Roberto; HAYASHIDA, Cesar Yoiti; AGUIAR-OLIVEIRA, Manuel H; et al. Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene. Journal of Clinical Endocrinology and Metabolism, Springfield, v. 84, n. 3, p. 917-923, 1998. -
APA
Salvatori, R., Hayashida, C. Y., Aguiar-Oliveira, M. H., Phillips III, J. A., Souza, A. H. O., Gondo, R. G., et al. (1998). Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene. Journal of Clinical Endocrinology and Metabolism, 84( 3), 917-923. -
NLM
Salvatori R, Hayashida CY, Aguiar-Oliveira MH, Phillips III JA, Souza AHO, Gondo RG, Toledo SPA, Conceição MM, Prince M, Maheshwari HG, Baumann G, Levine M. Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene. Journal of Clinical Endocrinology and Metabolism. 1998 ; 84( 3): 917-923. -
Vancouver
Salvatori R, Hayashida CY, Aguiar-Oliveira MH, Phillips III JA, Souza AHO, Gondo RG, Toledo SPA, Conceição MM, Prince M, Maheshwari HG, Baumann G, Levine M. Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene. Journal of Clinical Endocrinology and Metabolism. 1998 ; 84( 3): 917-923. - 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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