Mutational analysis of the gonadotropin-releasing hormone gene and its promoter in patients with congenital isolated hypogonadotropic hypogonadism (2006)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; TRARBACH, ERICKA BARBOSA - FM
- Unidade: FM
- Subjects: GONADOTROFINAS; HIPOGONADISMO (CONGÊNITO); MUTAÇÃO; RESUMOS (CONGRESSOS)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of pediatric endocrinology and metabolism
- ISSN: 0334-018X
- Volume/Número/Paginação/Ano: v. 19, n. suppl.3, p. 1085, res. 110, 2006
- Conference titles: Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP)
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ABNT
TRARBACH, E. B. et al. Mutational analysis of the gonadotropin-releasing hormone gene and its promoter in patients with congenital isolated hypogonadotropic hypogonadism. Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 18 abr. 2024. , 2006 -
APA
Trarbach, E. B., Costa, E. M. F., Mendonça, B. B. de, & Latronico, A. C. (2006). Mutational analysis of the gonadotropin-releasing hormone gene and its promoter in patients with congenital isolated hypogonadotropic hypogonadism. Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Trarbach EB, Costa EMF, Mendonça BB de, Latronico AC. Mutational analysis of the gonadotropin-releasing hormone gene and its promoter in patients with congenital isolated hypogonadotropic hypogonadism. Journal of pediatric endocrinology and metabolism. 2006 ; 19( suppl.3): 1085.[citado 2024 abr. 18 ] -
Vancouver
Trarbach EB, Costa EMF, Mendonça BB de, Latronico AC. Mutational analysis of the gonadotropin-releasing hormone gene and its promoter in patients with congenital isolated hypogonadotropic hypogonadism. Journal of pediatric endocrinology and metabolism. 2006 ; 19( suppl.3): 1085.[citado 2024 abr. 18 ] - An activating mutation in GPR54 gene causes gonadotropin-dependent precocious puberty
- A novel missense mutation of KISS1 gene mutation in a boy with idiopathic gonadotropin-dependent precocious puberty
- Uma nova mutação no gene GPR54 em dois irmãos com hipogonadismo hipogonadotrófico isolado normósmico
- Novas mutações no gene do receptor tipo 2 da proquineticina em pacientes com síndrome de Kallmann
- A GPR54-Activating Mutation in a Patient with Central Precocious Puberty
- Mutational analysis of TAC3 and TACR3 genes in children withidiopathic central precocious puberty
- Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
- Absense of duplication on DAX1 gene in patients with 46,XY sex reversal
- Crescimento linear e estatura final em crianças com tumores adrenais predominantemente virilizantes
- Absense of inactivating mutations and deletions of DAX1 gene in SRY negative 46,XX sex-reversed patients
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