Biochemical and molecular analysis of heterozygote individuals for classic '11-beta' hydroxylase deficiency due to 0356X mutation in the CYP11B1 gene (2004)
- Authors:
- USP affiliated authors: MOREIRA, AYRTON CUSTODIO - FMRP ; CASTRO, MARGARET DE - FMRP
- Unidade: FMRP
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher: International Society of Endocrinology
- Publisher place: London
- Date published: 2004
- Source:
- Título do periódico: Program and Abstracts
- Conference titles: International Congress of Endocrinology
-
ABNT
AMARAL, E. et al. Biochemical and molecular analysis of heterozygote individuals for classic '11-beta' hydroxylase deficiency due to 0356X mutation in the CYP11B1 gene. 2004, Anais.. London: International Society of Endocrinology, 2004. . Acesso em: 23 abr. 2024. -
APA
Amaral, E., Mello, M., Moreira, A. C., & Castro, M. de. (2004). Biochemical and molecular analysis of heterozygote individuals for classic '11-beta' hydroxylase deficiency due to 0356X mutation in the CYP11B1 gene. In Program and Abstracts. London: International Society of Endocrinology. -
NLM
Amaral E, Mello M, Moreira AC, Castro M de. Biochemical and molecular analysis of heterozygote individuals for classic '11-beta' hydroxylase deficiency due to 0356X mutation in the CYP11B1 gene. Program and Abstracts. 2004 ;[citado 2024 abr. 23 ] -
Vancouver
Amaral E, Mello M, Moreira AC, Castro M de. Biochemical and molecular analysis of heterozygote individuals for classic '11-beta' hydroxylase deficiency due to 0356X mutation in the CYP11B1 gene. Program and Abstracts. 2004 ;[citado 2024 abr. 23 ] - O gene homeobox Hexx1 nos defeitos da linha média cerebral (DLMC)
- Diagnóstico laboratorial da Síndorme de Cushing
- Efetio fundador da mutação Q356X no gene CYP11B1 em pacientes com deficiência da '11beta'- hidroxilase
- High frequence R337H mutation in TP53 in pediatric patients with sporadic adrenocortical tumor (ACT)
- Análise crítica do cortisol salivar na avaliação do eixo hipotálamo-hipófise-adrenal
- A palavra-chave do livro ... [Apresentação]
- Deficiência de 11'beta'-hidroxilase: análise bioquímica de indivíduos heterozigotos para mutação Q356X no gene CYP11B1
- Rsposta do cortisol salivar ao teste com oCRHNA na síndrome de cushing
- The homeobox HESXI gene in the midline cerebral defects (MCD)
- Familial glucocdorticoid deficiency due to a novel mutation of the ACTH receptor gene
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