Combined 17 alpha-hydroxylase/17,20 lyase deficiency in 11 brazilian patients:: biochemical diagnosis through progesterone levels confirmed by genotyping (2003)
- Authors:
- USP affiliated authors: MENDONCA, BERENICE BILHARINHO DE - FM ; LIN, CHIN AN - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2003
- Source:
- Título do periódico: Resumos
- Conference titles: ENDO - The Endocrine Society's Annual Meeting
-
ABNT
MARTIN, Regina M. et al. Combined 17 alpha-hydroxylase/17,20 lyase deficiency in 11 brazilian patients:: biochemical diagnosis through progesterone levels confirmed by genotyping. 2003, Anais.. Philadelphia: Faculdade de Medicina, Universidade de São Paulo, 2003. . Acesso em: 15 maio 2024. -
APA
Martin, R. M., Lin, C. J., Carrilho, A., Villar, H., Longui, C. A., & Mendonça, B. B. (2003). Combined 17 alpha-hydroxylase/17,20 lyase deficiency in 11 brazilian patients:: biochemical diagnosis through progesterone levels confirmed by genotyping. In Resumos. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Martin RM, Lin CJ, Carrilho A, Villar H, Longui CA, Mendonça BB. Combined 17 alpha-hydroxylase/17,20 lyase deficiency in 11 brazilian patients:: biochemical diagnosis through progesterone levels confirmed by genotyping. Resumos. 2003 ;[citado 2024 maio 15 ] -
Vancouver
Martin RM, Lin CJ, Carrilho A, Villar H, Longui CA, Mendonça BB. Combined 17 alpha-hydroxylase/17,20 lyase deficiency in 11 brazilian patients:: biochemical diagnosis through progesterone levels confirmed by genotyping. Resumos. 2003 ;[citado 2024 maio 15 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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