Source: Endocrine. Unidade: FM
Subjects: OVÁRIO, BRASILEIROS, EXPRESSÃO GÊNICA, DOENÇAS GENÉTICAS
ABNT
FRANCA, Monica M. et al. A novel homozygous 1-bp deletion in the NOBOX gene in two Brazilian sisters with primary ovarian failure. Endocrine, v. 58, n. 3, p. 442-447, 2017Tradução . . Disponível em: https://doi.org/10.1007/s12020-017-1459-2. Acesso em: 22 ago. 2024.APA
Franca, M. M., Funari, M. F. A., Lerario, A. M., Nishi, M. Y., Pita, C. C., Fontenele, E. G. P., & Mendonça, B. B. de. (2017). A novel homozygous 1-bp deletion in the NOBOX gene in two Brazilian sisters with primary ovarian failure. Endocrine, 58( 3), 442-447. doi:10.1007/s12020-017-1459-2NLM
Franca MM, Funari MFA, Lerario AM, Nishi MY, Pita CC, Fontenele EGP, Mendonça BB de. A novel homozygous 1-bp deletion in the NOBOX gene in two Brazilian sisters with primary ovarian failure [Internet]. Endocrine. 2017 ; 58( 3): 442-447.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1007/s12020-017-1459-2Vancouver
Franca MM, Funari MFA, Lerario AM, Nishi MY, Pita CC, Fontenele EGP, Mendonça BB de. A novel homozygous 1-bp deletion in the NOBOX gene in two Brazilian sisters with primary ovarian failure [Internet]. Endocrine. 2017 ; 58( 3): 442-447.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1007/s12020-017-1459-2