Molecular analysis of the hot spot area of the HSD3B2 gene in patientswith 3'beta'HSD deficiency (2003)
- Authors:
- USP affiliated authors: ELIAS, LUCILA LEICO KAGOHARA - FMRP ; MOREIRA, AYRTON CUSTODIO - FMRP ; CASTRO, MARGARET DE - FMRP
- Unidade: FMRP
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher: Endocrine Society
- Publisher place: Philadelphia
- Date published: 2003
- Source:
- Título do periódico: Program and Abstracts
- Conference titles: Annual Meeting of the Endocrine Society
-
ABNT
MERJO, Livia M. et al. Molecular analysis of the hot spot area of the HSD3B2 gene in patientswith 3'beta'HSD deficiency. 2003, Anais.. Philadelphia: Endocrine Society, 2003. . Acesso em: 24 abr. 2024. -
APA
Merjo, L. M., Elias, L. L. K., Amaral, F. C., Moreira, A. C., & Castro, M. de. (2003). Molecular analysis of the hot spot area of the HSD3B2 gene in patientswith 3'beta'HSD deficiency. In Program and Abstracts. Philadelphia: Endocrine Society. -
NLM
Merjo LM, Elias LLK, Amaral FC, Moreira AC, Castro M de. Molecular analysis of the hot spot area of the HSD3B2 gene in patientswith 3'beta'HSD deficiency. Program and Abstracts. 2003 ;[citado 2024 abr. 24 ] -
Vancouver
Merjo LM, Elias LLK, Amaral FC, Moreira AC, Castro M de. Molecular analysis of the hot spot area of the HSD3B2 gene in patientswith 3'beta'HSD deficiency. Program and Abstracts. 2003 ;[citado 2024 abr. 24 ] - Insuficiência adrenal primária no adulto: 150 anos depois de Addison
- Endocrine disorders in pediatric: onset langerhans cell histiocytosis
- Sensibilidade aos glicocorticóides (GC) em indivíduos normais
- A dose-response study of salivary cortisol after dexamethasone suppression test in Cushing's disease and its potential use in the differential diagnosis of Cushing's syndrome
- Glucocorticoid sensitivity in young healthy individuals: in vitro and in vivo studies
- Salivary cortisol response to overnight dexamethasone suppression test in the differential diagnosis of cushing syndrome
- Phenotype and genotype correlation of the microconversion from the CYP21A1P to the CYP21A2 gene in congenital adrenal hyperplasia
- Hiperplasia adrenal congênita (HAC) por deficiência da enzima 3'beta'-hidroxiesteróide desidrogenase (3'beta'HSD): análise bioquímica e genética
- Hiperplasia adrenal congênita (HAC) por deficiência da 3'beta'-hidroxisteroide desidrogenase (3'beta'HSD): análise e bioquímica e genética
- Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
