OTX2 gene mutations are rare in patients with combined pituitary hormone deficiency (CPHD) and /or midline cerebral defects (MCD) (2013)
- Authors:
- USP affiliated authors: CASTRO, MARGARET DE - FMRP ; MARTINELLI JUNIOR, CARLOS EDUARDO - FMRP ; ANTONINI, SONIR ROBERTO RAUBER - FMRP ; MOREIRA, AYRTON CUSTODIO - FMRP
- Unidade: FMRP
- Subjects: HORMÔNIOS HIPOFISÁRIOS (DEFICIÊNCIA); HORMÔNIOS DA ADENO-HIPÓFISE (DEFICIÊNCIA); GENES (ANÁLISE)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Trabalhos Científicos
- Conference titles: Congresso Brasileiro Pediátrico de Endocrinologia e Metabologia
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ABNT
NOVARETTI, N. et al. OTX2 gene mutations are rare in patients with combined pituitary hormone deficiency (CPHD) and /or midline cerebral defects (MCD). 2013, Anais.. Brasília: SBP, 2013. . Acesso em: 26 abr. 2024. -
APA
Novaretti, N., Santos, P. S., Moreira, A. C., Martinelli Junior, C. E., Igarashi, M., Ogata, T., et al. (2013). OTX2 gene mutations are rare in patients with combined pituitary hormone deficiency (CPHD) and /or midline cerebral defects (MCD). In Trabalhos Científicos. Brasília: SBP. -
NLM
Novaretti N, Santos PS, Moreira AC, Martinelli Junior CE, Igarashi M, Ogata T, Fukami M, Castro M de, Antonini SRR. OTX2 gene mutations are rare in patients with combined pituitary hormone deficiency (CPHD) and /or midline cerebral defects (MCD). Trabalhos Científicos. 2013 ;[citado 2024 abr. 26 ] -
Vancouver
Novaretti N, Santos PS, Moreira AC, Martinelli Junior CE, Igarashi M, Ogata T, Fukami M, Castro M de, Antonini SRR. OTX2 gene mutations are rare in patients with combined pituitary hormone deficiency (CPHD) and /or midline cerebral defects (MCD). Trabalhos Científicos. 2013 ;[citado 2024 abr. 26 ] - Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH-210HD)
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