Fonte: European Journal of Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
ABNT
HAYASHIDA, Cesar Yoiti et al. Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha. European Journal of Endocrinology, v. 142, n. 06, p. 557-563, 2000Tradução . . Disponível em: https://doi.org/10.1530/eje.0.1420557. Acesso em: 04 out. 2024.APA
Hayashida, C. Y., Gondo, R. G., Ferrari, C., Toledo, S. P. A., Salvatori, R., Levine, M. A., et al. (2000). Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha. European Journal of Endocrinology, 142( 06), 557-563. doi:10.1530/eje.0.1420557NLM
Hayashida CY, Gondo RG, Ferrari C, Toledo SPA, Salvatori R, Levine MA, Ezabella MCL, Abelin N, Gianella Neto D, Wajchenberg BL. Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha [Internet]. European Journal of Endocrinology. 2000 ; 142( 06): 557-563.[citado 2024 out. 04 ] Available from: https://doi.org/10.1530/eje.0.1420557Vancouver
Hayashida CY, Gondo RG, Ferrari C, Toledo SPA, Salvatori R, Levine MA, Ezabella MCL, Abelin N, Gianella Neto D, Wajchenberg BL. Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha [Internet]. European Journal of Endocrinology. 2000 ; 142( 06): 557-563.[citado 2024 out. 04 ] Available from: https://doi.org/10.1530/eje.0.1420557