Fonte: The Journal of Clinical Endocrinology & Metabolism. Unidade: FMRP
Assuntos: DOENÇAS CONGÊNITAS, MUTAÇÃO GENÉTICA, HORMÔNIO LIBERADOR DE HORMÔNIO DE CRESCIMENTO
ABNT
SANTOS, Alécia A. Oliveira et al. Enteroendocrine connections in congenital isolated GH deficiency due to a GHRH receptor gene mutation. The Journal of Clinical Endocrinology & Metabolism, v. 104, n. 7, p. 2777-2784, 2019Tradução . . Disponível em: https://doi.org/10.1210/jc.2019-00094. Acesso em: 30 ago. 2024.APA
Santos, A. A. O., Salvatori, R., Nogueira, M. C., Arruda, A. C. B. de Q., Barros-Oliveira, C. S., Leal, Â. C. G. B., et al. (2019). Enteroendocrine connections in congenital isolated GH deficiency due to a GHRH receptor gene mutation. The Journal of Clinical Endocrinology & Metabolism, 104( 7), 2777-2784. doi:10.1210/jc.2019-00094NLM
Santos AAO, Salvatori R, Nogueira MC, Arruda ACB de Q, Barros-Oliveira CS, Leal ÂCGB, Marinho CG, Damascena NP, Oliveira DA, Melo MA, Oliveira CRP, Costa FO da, Santos JSS dos, Santos PFC, Campos VC, Santos EG, Melo EV de, Barbosa MLA, Rocha IES, Castro M de, Oliveira MH de A. Enteroendocrine connections in congenital isolated GH deficiency due to a GHRH receptor gene mutation [Internet]. The Journal of Clinical Endocrinology & Metabolism. 2019 ; 104( 7): 2777-2784.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1210/jc.2019-00094Vancouver
Santos AAO, Salvatori R, Nogueira MC, Arruda ACB de Q, Barros-Oliveira CS, Leal ÂCGB, Marinho CG, Damascena NP, Oliveira DA, Melo MA, Oliveira CRP, Costa FO da, Santos JSS dos, Santos PFC, Campos VC, Santos EG, Melo EV de, Barbosa MLA, Rocha IES, Castro M de, Oliveira MH de A. Enteroendocrine connections in congenital isolated GH deficiency due to a GHRH receptor gene mutation [Internet]. The Journal of Clinical Endocrinology & Metabolism. 2019 ; 104( 7): 2777-2784.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1210/jc.2019-00094