Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH-210HD) (2012)
- Authors:
- USP affiliated authors: MARTINELLI JUNIOR, CARLOS EDUARDO - FMRP ; MOREIRA, AYRTON CUSTODIO - FMRP ; ANTONINI, SONIR ROBERTO RAUBER - FMRP ; CASTRO, MARGARET DE - FMRP
- Unidade: FMRP
- Subjects: HIPERPLASIA SUPRARRENAL CONGÊNITA; HIDROXILASE (DEFICIÊNCIA)
- Language: Inglês
- Imprenta:
- Source:
- Título: Endocrine Abstracts
- ISSN: 1470-3947
- Volume/Número/Paginação/Ano: v. 29, 2012
- Conference titles: International Congress of Endocrinology
-
ABNT
COELI, F. et al. Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH-210HD). Endocrine Abstracts. Woodlands: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 14 nov. 2024. , 2012 -
APA
Coeli, F., Turatti, W., Elias, P., Martinelli Junior, C. E., Moreira, A. C., Antonini, S. R. R., & Castro, M. de. (2012). Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH-210HD). Endocrine Abstracts. Woodlands: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Coeli F, Turatti W, Elias P, Martinelli Junior CE, Moreira AC, Antonini SRR, Castro M de. Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH-210HD). Endocrine Abstracts. 2012 ; 29[citado 2024 nov. 14 ] -
Vancouver
Coeli F, Turatti W, Elias P, Martinelli Junior CE, Moreira AC, Antonini SRR, Castro M de. Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH-210HD). Endocrine Abstracts. 2012 ; 29[citado 2024 nov. 14 ] - OTX2 gene mutations are rare in patients with combined pituitary hormone deficiency (CPHD) and /or midline cerebral defects (MCD)
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