Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome (2007)
- Authors:
- Autor USP: CASTRO, MARGARET DE - FMRP
- Unidade: FMRP
- Assunto: HIPOGONADISMO
- Language: Inglês
- Imprenta:
- Source:
- Título: Program and Abstracts
- Conference titles: The Endocrine Society's Annual Meeting (ENDO)
-
ABNT
ABREU, Ana Paula et al. Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. 2007, Anais.. Toronto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2007. . Acesso em: 15 fev. 2026. -
APA
Abreu, A. P., Trarbach, E., Castro, M. de, Costa, E. M. F., Versiani, B., Baptista, M. T. M., et al. (2007). Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. In Program and Abstracts. Toronto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Abreu AP, Trarbach E, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. Program and Abstracts. 2007 ;[citado 2026 fev. 15 ] -
Vancouver
Abreu AP, Trarbach E, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. Program and Abstracts. 2007 ;[citado 2026 fev. 15 ] - TAC3/TACR3 mutations reveal preferential activation of GnRH release by neurokinin B in neonatal life followed by reversal in adulthood
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