Mutation analysis of NANOS3 in Brazilian women with primary ovarian failure (2016)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- DOI: 10.6061/clinics/2016(12)03
- Subjects: BRASILEIROS; AMENORREIA; DIFERENCIAÇÃO SEXUAL (NÚCLEO CELULAR)
- Language: Inglês
- Imprenta:
- Source:
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
SOUSA, Braian Lucas A. et al. Mutation analysis of NANOS3 in Brazilian women with primary ovarian failure. Clinics, v. 71, n. 12, p. 695-698, 2016Tradução . . Disponível em: https://doi.org/10.6061/clinics/2016(12)03. Acesso em: 26 abr. 2024. -
APA
Sousa, B. L. A., Nishi, M. Y., Santos, M. G., Brito, V. N., Domenice, S., & Mendonca, B. B. (2016). Mutation analysis of NANOS3 in Brazilian women with primary ovarian failure. Clinics, 71( 12), 695-698. doi:10.6061/clinics/2016(12)03 -
NLM
Sousa BLA, Nishi MY, Santos MG, Brito VN, Domenice S, Mendonca BB. Mutation analysis of NANOS3 in Brazilian women with primary ovarian failure [Internet]. Clinics. 2016 ; 71( 12): 695-698.[citado 2024 abr. 26 ] Available from: https://doi.org/10.6061/clinics/2016(12)03 -
Vancouver
Sousa BLA, Nishi MY, Santos MG, Brito VN, Domenice S, Mendonca BB. Mutation analysis of NANOS3 in Brazilian women with primary ovarian failure [Internet]. Clinics. 2016 ; 71( 12): 695-698.[citado 2024 abr. 26 ] Available from: https://doi.org/10.6061/clinics/2016(12)03 - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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- Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitibity syndrome in a brazilian cohort: five novel mutations in the androgen receptor gene
- Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
- Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect
- Padrão de resposta do TSH após estímulo com TRH em pacientes com hipotireoidismo hipofisário devido a mutações nos genes HESX1, PROP1 e PIT1
Informações sobre o DOI: 10.6061/clinics/2016(12)03 (Fonte: oaDOI API)
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