Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? (2010)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; BACHEGA, TÂNIA APARECIDA SARTORI SANCHEZ - FM
- Unidades: FM; FM
- Subjects: FENÓTIPOS (VARIABILIDADE); HIDROXILASE (DEFICIÊNCIA); ALELOPATIA; GENÓTIPOS (VARIABILIDADE); TRANSTORNOS DA MENSTRUAÇÃO; PUBERDADE PRECOCE; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Conference title: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP"
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ABNT
MOURA, V O; PACHECO, M; MADUREIRA, G; et al. Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? Clinics[S.l: s.n.], 2010. -
APA
Moura, V. O., Pacheco, M., Madureira, G., Marcondes, J. A. M., Mendonça, B. B. de, & Bachega, T. A. S. S. (2010). Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? Clinics. São Paulo. -
NLM
Moura VO, Pacheco M, Madureira G, Marcondes JAM, Mendonça BB de, Bachega TASS. Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? Clinics. 2010 ; 65 S70. -
Vancouver
Moura VO, Pacheco M, Madureira G, Marcondes JAM, Mendonça BB de, Bachega TASS. Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? Clinics. 2010 ; 65 S70. - Classic congenital adrenal hyperplasia and its impact on reproduction
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- The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene
- Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia
- Impact of Glucocorticoid Receptor Gene Polymorphisms on the Metabolic Profile of Adult Patients with the Classical Form of 21-Hydroxylase Deficiency
- Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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