Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: CRIANÇAS, POLIMORFISMO, HIPOTIROIDISMO (ETIOLOGIA)
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ABNT
ALVA, Catarina B. d et al. Absence of mutations in the follicle-stimulating hormone receptor gene in children with primary hypothyroidism and gonadal hyperstimulation. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 29 set. 2024.APA
Alva, C. B. d, Suarez, E., Latronico, A. C., & Mendonça, B. B. (2005). Absence of mutations in the follicle-stimulating hormone receptor gene in children with primary hypothyroidism and gonadal hyperstimulation. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.NLM
Alva CB d, Suarez E, Latronico AC, Mendonça BB. Absence of mutations in the follicle-stimulating hormone receptor gene in children with primary hypothyroidism and gonadal hyperstimulation. Program and Abstracts. 2005 ;[citado 2024 set. 29 ]Vancouver
Alva CB d, Suarez E, Latronico AC, Mendonça BB. Absence of mutations in the follicle-stimulating hormone receptor gene in children with primary hypothyroidism and gonadal hyperstimulation. Program and Abstracts. 2005 ;[citado 2024 set. 29 ]