Fonte: Program and Abstracts Book. Nome do evento: Annual Meeting of the Endocrine Society. Unidades: FMRP, FM
Assuntos: MUTAÇÃO GENÉTICA, GONADOTROFINAS
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 ago. 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 ago. 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 ago. 26 ]