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Filtros : "Moraes, Daniela Rodrigues" Limpar

Filtros

USP affiliated authors
- mendonça, berenice bilharinho de (~2)
- jorge, alexander augusto de lima (~1)
- montenegro, luciana ribeiro (~1)
Date published
- 2022 (~1)
- 2017 (~1)
Subjects
- andrógenos (1)
- crianças (1)
- desenvolvimento sexual (1)
- diagnóstico por imagem (1)
- doenças genéticas (1)

Artigo de periodico
Contribution of Clinical and Genetic Approaches for Diagnosing 209 Index Cases With 46,XY Differences of Sex Development (2022)
Gomes, Nathalia Lisboa; Batista, Rafael Loch; Nishi, Mirian Y.; Lerario, Antonio Marcondes; Silva, Thatiana E.; Narcizo, Amanda de Moraes; Benedetti, Anna Flavia Figueredo; Funari, Mariana Ferreira de Assis; Faria Junior, Jose Antonio; Moraes, Daniela Rodrigues; Montenegro, Luciana Ribeiro; Jorge, Alexander Augusto de Lima ; Mendonca, Berenice Bilharinho de
Source: Journal of clinical endocrinology & metabolism. Unidade: FM
Subjects: CRIANÇAS, SINAIS E SINTOMAS, DOENÇAS GENÉTICAS, DIAGNÓSTICO POR IMAGEM
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, Nathalia Lisboa et al. Contribution of Clinical and Genetic Approaches for Diagnosing 209 Index Cases With 46,XY Differences of Sex Development. Journal of clinical endocrinology & metabolism, v. 107, n. 5, p. E1797-E1806, 2022Tradução . . Disponível em: https://doi.org/10.1210/clinem/dgac064. Acesso em: 01 nov. 2024.
APA
Gomes, N. L., Batista, R. L., Nishi, M. Y., Lerario, A. M., Silva, T. E., Narcizo, A. de M., et al. (2022). Contribution of Clinical and Genetic Approaches for Diagnosing 209 Index Cases With 46,XY Differences of Sex Development. Journal of clinical endocrinology & metabolism, 107( 5), E1797-E1806. doi:10.1210/clinem/dgac064
NLM
Gomes NL, Batista RL, Nishi MY, Lerario AM, Silva TE, Narcizo A de M, Benedetti AFF, Funari MF de A, Faria Junior JA, Moraes DR, Montenegro LR, Jorge AA de L, Mendonca BB de. Contribution of Clinical and Genetic Approaches for Diagnosing 209 Index Cases With 46,XY Differences of Sex Development [Internet]. Journal of clinical endocrinology & metabolism. 2022 ; 107( 5): E1797-E1806.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1210/clinem/dgac064
Vancouver
Gomes NL, Batista RL, Nishi MY, Lerario AM, Silva TE, Narcizo A de M, Benedetti AFF, Funari MF de A, Faria Junior JA, Moraes DR, Montenegro LR, Jorge AA de L, Mendonca BB de. Contribution of Clinical and Genetic Approaches for Diagnosing 209 Index Cases With 46,XY Differences of Sex Development [Internet]. Journal of clinical endocrinology & metabolism. 2022 ; 107( 5): E1797-E1806.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1210/clinem/dgac064
Artigo de periodico
A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome (2017)
Batista, Rafael Loch; Rodrigues, Andresa di Santi; Nishi, Miriam Yumie; Gomes, Nathalia Lisboa; Faria Junior, José Antonio Diniz; Moraes, Daniela Rodrigues; Carvalho, Luciani Renata; Costa, Elaine Maria Frede; Domenice, Sorahia; Mendonça, Berenice Bilharinho de
Source: The Journal of Steroid Biochemistry and Molecular Biology. Unidade: FM
Subjects: ANDRÓGENOS, RECEPTORES ANDROGÊNICOS, MUTAÇÃO GENÉTICA, DESENVOLVIMENTO SEXUAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BATISTA, Rafael Loch et al. A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome. The Journal of Steroid Biochemistry and Molecular Biology, v. 174, p. 14-16, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.jsbmb.2017.07.020. Acesso em: 01 nov. 2024.
APA
Batista, R. L., Rodrigues, A. di S., Nishi, M. Y., Gomes, N. L., Faria Junior, J. A. D., Moraes, D. R., et al. (2017). A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome. The Journal of Steroid Biochemistry and Molecular Biology, 174, 14-16. doi:10.1016/j.jsbmb.2017.07.020
NLM
Batista RL, Rodrigues A di S, Nishi MY, Gomes NL, Faria Junior JAD, Moraes DR, Carvalho LR, Costa EMF, Domenice S, Mendonça BB de. A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome [Internet]. The Journal of Steroid Biochemistry and Molecular Biology. 2017 ; 174 14-16.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.jsbmb.2017.07.020
Vancouver
Batista RL, Rodrigues A di S, Nishi MY, Gomes NL, Faria Junior JAD, Moraes DR, Carvalho LR, Costa EMF, Domenice S, Mendonça BB de. A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome [Internet]. The Journal of Steroid Biochemistry and Molecular Biology. 2017 ; 174 14-16.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.jsbmb.2017.07.020

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