Novel FGF8 gene mutations in patients with congenital isolated isolated hypogonadotropic hypogonadism (2008)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; XAVIER, ANA CLAUDIA LATRÔNICO - FM
- Unidade: FM
- Subjects: HIPOGONADISMO; MUTAÇÃO GENÉTICA; SÍNDROME DE KALLMANN
- Language: Inglês
- Imprenta:
- Source:
- Título: Arquivos Brasileiros de Endocrinologia e Metabologia
- ISSN: 0004-2730
- Volume/Número/Paginação/Ano: v. 52, supl. 6, parte II, p. S793, res. OP-095, 2008
- Conference titles: International Congress of Endocrinology
-
ABNT
TRARBACH, E. B. et al. Novel FGF8 gene mutations in patients with congenital isolated isolated hypogonadotropic hypogonadism. Arquivos Brasileiros de Endocrinologia e Metabologia. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 03 out. 2024. , 2008 -
APA
Trarbach, E. B., Teles, M. G., Costa, E. M. F., Abreu, A. P., Mendonça, B. B., Castro, M., et al. (2008). Novel FGF8 gene mutations in patients with congenital isolated isolated hypogonadotropic hypogonadism. Arquivos Brasileiros de Endocrinologia e Metabologia. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Trarbach EB, Teles MG, Costa EMF, Abreu AP, Mendonça BB, Castro M, Guerra G, Garmes HM, Baptista MTM, Latronico ACX. Novel FGF8 gene mutations in patients with congenital isolated isolated hypogonadotropic hypogonadism. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52 S793.[citado 2024 out. 03 ] -
Vancouver
Trarbach EB, Teles MG, Costa EMF, Abreu AP, Mendonça BB, Castro M, Guerra G, Garmes HM, Baptista MTM, Latronico ACX. Novel FGF8 gene mutations in patients with congenital isolated isolated hypogonadotropic hypogonadism. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52 S793.[citado 2024 out. 03 ] - Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life
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