Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2 (2008)
- Authors:
- USP affiliated authors: CASTRO, MARGARET DE - FMRP ; MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidades: FMRP; FM
- Subjects: MUTAÇÃO GENÉTICA; GONADOTROFINAS
- Language: Inglês
- Imprenta:
- Publisher place: San Francisco
- Date published: 2008
- Source:
- Título do periódico: Program and Abstracts Book
- Conference titles: Annual Meeting of the Endocrine Society
-
ABNT
ABREU, A. P. et al. Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2. 2008, Anais.. San Francisco: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2008. . Acesso em: 26 abr. 2024. -
APA
Abreu, A. P., Trarbach, E. B., Castro, M. de, Costa, E. M. F., Versiani, B., Guerra Júnior, G., et al. (2008). Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2. In Program and Abstracts Book. San Francisco: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Abreu AP, Trarbach EB, Castro M de, Costa EMF, Versiani B, Guerra Júnior G, Baptista MTM, Garmes HM, Mendonça BB de, Latronico AC. Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2. Program and Abstracts Book. 2008 ;[citado 2024 abr. 26 ] -
Vancouver
Abreu AP, Trarbach EB, Castro M de, Costa EMF, Versiani B, Guerra Júnior G, Baptista MTM, Garmes HM, Mendonça BB de, Latronico AC. Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2. Program and Abstracts Book. 2008 ;[citado 2024 abr. 26 ] - Clinical and molecular analysis of TAC3 and TACR3 genes in Brazilian patients with isolated hypogonadotropic hypogonadism
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