The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants (2011)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- DOI: 10.1159/000316536
- Subjects: MUTAÇÃO GENÉTICA; TRANSTORNOS GONADAIS; CROMOSSOMOS SEXUAIS (FISIOPATOLOGIA)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Hormone Research in Paediatrics
- ISSN: 1663-2818
- Volume/Número/Paginação/Ano: v. 75, n. 1, p. 26-31, 2011
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
NISHI, Mirian Yumie; COSTA, Elaine Maria Frade; OLIVEIRA, Suely Beirão; MENDONCA, Berenice Bilharinho; DOMENICE, Sorahia. The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants. Hormone Research in Paediatrics, Basel, v. 75, n. 1, p. 26-31, 2011. Disponível em: < http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=316536&Ausgabe=254824&ProduktNr=224036&filename=316536.pdf > DOI: 10.1159/000316536. -
APA
Nishi, M. Y., Costa, E. M. F., Oliveira, S. B., Mendonca, B. B., & Domenice, S. (2011). The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants. Hormone Research in Paediatrics, 75( 1), 26-31. doi:10.1159/000316536 -
NLM
Nishi MY, Costa EMF, Oliveira SB, Mendonca BB, Domenice S. The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants [Internet]. Hormone Research in Paediatrics. 2011 ; 75( 1): 26-31.Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=316536&Ausgabe=254824&ProduktNr=224036&filename=316536.pdf -
Vancouver
Nishi MY, Costa EMF, Oliveira SB, Mendonca BB, Domenice S. The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants [Internet]. Hormone Research in Paediatrics. 2011 ; 75( 1): 26-31.Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=316536&Ausgabe=254824&ProduktNr=224036&filename=316536.pdf - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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Informações sobre o DOI: 10.1159/000316536 (Fonte: oaDOI API)
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