Fonte: Journal of pediatric endocrinology and metabolism. Nome do evento: Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP). Unidade: FM
Assuntos: HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA), DELEÇÃO DE GENES, GLÂNDULA PITUITÁRIA (FISIOPATOLOGIA), AMPLIFICAÇÃO DE GENES, RESUMOS (CONGRESSOS)
ABNT
ABRAO, M. G. et al. Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD). Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2004APA
Abrao, M. G., Carvalho, L., Leite, M. V., Nishi, M., Barbosa, A., Arnhold, I. J. P., & Mendonça, B. B. (2004). Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD). Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo.NLM
Abrao MG, Carvalho L, Leite MV, Nishi M, Barbosa A, Arnhold IJP, Mendonça BB. Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD). Journal of pediatric endocrinology and metabolism. 2004 ; 17( suppl.5): 1345.[citado 2024 nov. 01 ]Vancouver
Abrao MG, Carvalho L, Leite MV, Nishi M, Barbosa A, Arnhold IJP, Mendonça BB. Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD). Journal of pediatric endocrinology and metabolism. 2004 ; 17( suppl.5): 1345.[citado 2024 nov. 01 ]