Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD) (2004)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA); DELEÇÃO DE GENES; GLÂNDULA PITUITÁRIA (FISIOPATOLOGIA); AMPLIFICAÇÃO DE GENES; RESUMOS (CONGRESSOS)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of pediatric endocrinology and metabolism
- ISSN: 0334-018X
- Volume/Número/Paginação/Ano: v. 17, n. suppl.5, p. 1345, res. Poster 1, 2004
- Conference titles: Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP)
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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 jun. 2024. , 2004 -
APA
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 jun. 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 jun. 01 ] - Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
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