Mutational analysis of the gonadotropin-releasing hormone gene and its promoter in patients with congenital isolated hypogonadotropic hypogonadism (2006)
- Autores:
- Autores USP: MENDONÇA, BERENICE BILHARINHO DE - FM ; TRARBACH, ERICKA BARBOSA - FM
- Unidade: FM
- Assuntos: GONADOTROFINAS; HIPOGONADISMO (CONGÊNITO); MUTAÇÃO; RESUMOS (CONGRESSOS)
- Idioma: Inglês
- Imprenta:
- Fonte:
- 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
- Nome do evento: 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: 10 ago. 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 ago. 10 ] -
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 ago. 10 ] - 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
- Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
- Reavaliação na idade adulta do diagnóstico da deficiência de GH (DGH) determinado na infância
- Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty
- Missense mutation a300v in the DAX1 gene in a Brazilian male with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism
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