Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care (2016)
- Authors:
- USP affiliated authors: MOREIRA, AYRTON CUSTODIO - FMRP ; CASTRO, MARGARET DE - FMRP ; ANTONINI, SONIR ROBERTO RAUBER - FMRP
- Unidade: FMRP
- DOI: 10.1159/000447515
- Subjects: PUBERDADE PRECOCE; MUTAÇÃO GENÉTICA; AMINOÁCIDOS
- Keywords: Gonadotropin-dependent precocious puberty; MKRN3 mutation; Penetrance; Early diagnosis; Genetic counseling
- Language: Inglês
- Imprenta:
- Source:
- Título: Hormone Research in Paediatrics
- ISSN: 1663-2818
- Volume/Número/Paginação/Ano: v. 86, n. 2, p. 126-130, 2016
- Status:
- Artigo possui acesso gratuito no site do editor (Bronze Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
STECCHINI, Monica F. et al. Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care. Hormone Research in Paediatrics, v. 86, n. 2, p. 126-130, 2016Tradução . . Disponível em: https://doi.org/10.1159/000447515. Acesso em: 31 mar. 2026. -
APA
Stecchini, M. F., Macedo, D. B., Reis, A. C. S., Abreu, A. P., Moreira, A. C., Castro, M. de, et al. (2016). Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care. Hormone Research in Paediatrics, 86( 2), 126-130. doi:10.1159/000447515 -
NLM
Stecchini MF, Macedo DB, Reis ACS, Abreu AP, Moreira AC, Castro M de, Kaiser UB, Latronico AC, Antonini SRR. Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care [Internet]. Hormone Research in Paediatrics. 2016 ; 86( 2): 126-130.[citado 2026 mar. 31 ] Available from: https://doi.org/10.1159/000447515 -
Vancouver
Stecchini MF, Macedo DB, Reis ACS, Abreu AP, Moreira AC, Castro M de, Kaiser UB, Latronico AC, Antonini SRR. Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care [Internet]. Hormone Research in Paediatrics. 2016 ; 86( 2): 126-130.[citado 2026 mar. 31 ] Available from: https://doi.org/10.1159/000447515 - Commom polymorphisms in GHRd3, IGFBP3 and IGF1 genes do not explain GH-IGF-I dissociation in treated acromegalic patients
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