Source: Hormone Research. Conference titles: European Society for Paediatric Endocrinology (ESPE). Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, HORMÔNIO DO CRESCIMENTO (ANORMALIDADES), RESUMOS (EVENTOS)
ABNT
CARVALHO, Luciani et al. Homozygous mutations in the promoter region of growth hormone gene (GH1) in 3 siblings is associated with isolated growth hormone deficiency (IGHD). Hormone Research. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 23 out. 2025. , 2008APA
Carvalho, L., Jorge, A., Martin, R. M., Franca, M. C., Mendonça, B. B., Costalongo, E. F., et al. (2008). Homozygous mutations in the promoter region of growth hormone gene (GH1) in 3 siblings is associated with isolated growth hormone deficiency (IGHD). Hormone Research. Basel: Faculdade de Medicina, Universidade de São Paulo.NLM
Carvalho L, Jorge A, Martin RM, Franca MC, Mendonça BB, Costalongo EF, Montenegro LR, Arnhold IJP. Homozygous mutations in the promoter region of growth hormone gene (GH1) in 3 siblings is associated with isolated growth hormone deficiency (IGHD). Hormone Research. 2008 ; 70 20.[citado 2025 out. 23 ]Vancouver
Carvalho L, Jorge A, Martin RM, Franca MC, Mendonça BB, Costalongo EF, Montenegro LR, Arnhold IJP. Homozygous mutations in the promoter region of growth hormone gene (GH1) in 3 siblings is associated with isolated growth hormone deficiency (IGHD). Hormone Research. 2008 ; 70 20.[citado 2025 out. 23 ]