Molecular and Genetic Aspects of Congenital Isolated Hypogonadotropic Hypogonadism (2017)
Source: Endocrinology and metabolism clinics of north america. Unidade: FM
Subjects: OLFATO, DOENÇAS CONGÊNITAS, TRANSTORNOS GONADAIS, HORMÔNIO LIBERADOR DE GONADOTROFINAS, SÍNDROME DE KALLMANN
ABNT
AMATO, Lorena Guimaraes Lima e LATRONICO, Ana Claudia e SILVEIRA, Leticia Ferreira Gontijo. Molecular and Genetic Aspects of Congenital Isolated Hypogonadotropic Hypogonadism. Endocrinology and metabolism clinics of north america, v. 46, n. 2, p. 283-303, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ecl.2017.01.010. Acesso em: 04 jun. 2024.APA
Amato, L. G. L., Latronico, A. C., & Silveira, L. F. G. (2017). Molecular and Genetic Aspects of Congenital Isolated Hypogonadotropic Hypogonadism. Endocrinology and metabolism clinics of north america, 46( 2), 283-303. doi:10.1016/j.ecl.2017.01.010NLM
Amato LGL, Latronico AC, Silveira LFG. Molecular and Genetic Aspects of Congenital Isolated Hypogonadotropic Hypogonadism [Internet]. Endocrinology and metabolism clinics of north america. 2017 ; 46( 2): 283-303.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1016/j.ecl.2017.01.010Vancouver
Amato LGL, Latronico AC, Silveira LFG. Molecular and Genetic Aspects of Congenital Isolated Hypogonadotropic Hypogonadism [Internet]. Endocrinology and metabolism clinics of north america. 2017 ; 46( 2): 283-303.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1016/j.ecl.2017.01.010