Source: Program & Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FMRP
Subjects: GLÂNDULAS ENDÓCRINAS, SÍNDROME DE KALLMANN
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TRARBACH, Ericka B. et al. Novel FGFR1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia. 2006, Anais.. Massachusetts: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2006. . Acesso em: 06 nov. 2024.APA
Trarbach, E. B., Costa, E. M. F., Versiani, B. R., Castro, M., Baptista, M. T. M., Garmes, H. M., et al. (2006). Novel FGFR1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia. In Program & Abstracts. Massachusetts: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.NLM
Trarbach EB, Costa EMF, Versiani BR, Castro M, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Novel FGFR1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia. Program & Abstracts. 2006 ;[citado 2024 nov. 06 ]Vancouver
Trarbach EB, Costa EMF, Versiani BR, Castro M, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Novel FGFR1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia. Program & Abstracts. 2006 ;[citado 2024 nov. 06 ]
