Source: European Journal of Endocrinology. Unidade: FM
Subjects: HIPOGONADISMO (GENÉTICO;CONGÊNITO), PUBERDADE (DESENVOLVIMENTO), HORMÔNIO LUTEINIZANTE (SECREÇÃO), HIPOTÁLAMO (FISIOPATOLOGIA), GENES, HORMÔNIO FOLÍCULO-ESTIMULANTE (SECREÇÃO)
ABNT
BENEDUZZI, Daiane et al. Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, v. 165, n. 2, p. 145-150, 2011Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-0199. Acesso em: 10 out. 2024.APA
Beneduzzi, D., Iyer, A. K., Trarbach, E. B., Silveira-Neto, A. P., Silveira, L. G., Tusset, C., et al. (2011). Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, 165( 2), 145-150. doi:10.1530/EJE-11-0199NLM
Beneduzzi D, Iyer AK, Trarbach EB, Silveira-Neto AP, Silveira LG, Tusset C, Yip K, Mendonça BB, Mellon PL, Latronico AC. Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2011 ; 165( 2): 145-150.[citado 2024 out. 10 ] Available from: https://doi.org/10.1530/EJE-11-0199Vancouver
Beneduzzi D, Iyer AK, Trarbach EB, Silveira-Neto AP, Silveira LG, Tusset C, Yip K, Mendonça BB, Mellon PL, Latronico AC. Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2011 ; 165( 2): 145-150.[citado 2024 out. 10 ] Available from: https://doi.org/10.1530/EJE-11-0199