Absence of mutations in the promoter STAT5B binding sites of the insulin-like growth factor-I (IGF-I) gene in patients born small for gestacional ace (SGA) or with idiopathic short stature (ISS) (2006)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: RECÉM-NASCIDO DE BAIXO PESO; FATORES DE RISCO; MUTAÇÃO; PESO-ESTATURA; RESUMOS (CONGRESSOS)
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of pediatric endocrinology and metabolism
- ISSN: 0334-018X
- Volume/Número/Paginação/Ano: v. 19, n. suppl.3, p. 1079, res. 82, 2006
- Conference titles: Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP)
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ABNT
MONTENEGRO, L. R. et al. Absence of mutations in the promoter STAT5B binding sites of the insulin-like growth factor-I (IGF-I) gene in patients born small for gestacional ace (SGA) or with idiopathic short stature (ISS). Journal of pediatric endocrinology and metabolism, v. 19, n. suppl.3, p. 1079, 2006Tradução . . Acesso em: 08 out. 2024. -
APA
Montenegro, L. R., Liborio, D. C. C., Arnhold, I., Mendonça, B. B. de, & Jorge, A. A. L. (2006). Absence of mutations in the promoter STAT5B binding sites of the insulin-like growth factor-I (IGF-I) gene in patients born small for gestacional ace (SGA) or with idiopathic short stature (ISS). Journal of pediatric endocrinology and metabolism, 19( suppl.3), 1079. -
NLM
Montenegro LR, Liborio DCC, Arnhold I, Mendonça BB de, Jorge AAL. Absence of mutations in the promoter STAT5B binding sites of the insulin-like growth factor-I (IGF-I) gene in patients born small for gestacional ace (SGA) or with idiopathic short stature (ISS). Journal of pediatric endocrinology and metabolism. 2006 ; 19( suppl.3): 1079.[citado 2024 out. 08 ] -
Vancouver
Montenegro LR, Liborio DCC, Arnhold I, Mendonça BB de, Jorge AAL. Absence of mutations in the promoter STAT5B binding sites of the insulin-like growth factor-I (IGF-I) gene in patients born small for gestacional ace (SGA) or with idiopathic short stature (ISS). Journal of pediatric endocrinology and metabolism. 2006 ; 19( suppl.3): 1079.[citado 2024 out. 08 ] - Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
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