46,XY disorder of sex development (DSD) due to 17b-hydroxysteroid dehydrogenase type 3 deficiency (2017)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; CARVALHO, FILOMENA MARINO - FM
- Unidade: FM
- DOI: 10.1016/j.jsbmb.2016.05.002
- Subjects: TRANSTORNOS DA DIFERENCIAÇÃO SEXUAL; TESTOSTERONA; GENITÁLIA; CARCINOGÊNESE
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: The Journal of Steroid Biochemistry and Molecular Biology
- ISSN: 0960-0760
- Volume/Número/Paginação/Ano: v. 165, p. 79-85, 2017
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
MENDONÇA, Berenice B. et al. 46,XY disorder of sex development (DSD) due to 17b-hydroxysteroid dehydrogenase type 3 deficiency. The Journal of Steroid Biochemistry and Molecular Biology, v. 165, p. 79-85, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.jsbmb.2016.05.002. Acesso em: 23 abr. 2024. -
APA
Mendonça, B. B., Gomes, N. L., Domenice, S., Costa, E. M. F., Inacio, M., Martin, R. M., et al. (2017). 46,XY disorder of sex development (DSD) due to 17b-hydroxysteroid dehydrogenase type 3 deficiency. The Journal of Steroid Biochemistry and Molecular Biology, 165, 79-85. doi:10.1016/j.jsbmb.2016.05.002 -
NLM
Mendonça BB, Gomes NL, Domenice S, Costa EMF, Inacio M, Martin RM, Nishi MY, Carvalho FM, Tibor FD. 46,XY disorder of sex development (DSD) due to 17b-hydroxysteroid dehydrogenase type 3 deficiency [Internet]. The Journal of Steroid Biochemistry and Molecular Biology. 2017 ; 165 79-85.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.jsbmb.2016.05.002 -
Vancouver
Mendonça BB, Gomes NL, Domenice S, Costa EMF, Inacio M, Martin RM, Nishi MY, Carvalho FM, Tibor FD. 46,XY disorder of sex development (DSD) due to 17b-hydroxysteroid dehydrogenase type 3 deficiency [Internet]. The Journal of Steroid Biochemistry and Molecular Biology. 2017 ; 165 79-85.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.jsbmb.2016.05.002 - A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with denys-Drash syndrome
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Informações sobre o DOI: 10.1016/j.jsbmb.2016.05.002 (Fonte: oaDOI API)
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