Allelic variants of the GABA-A receptor alpha-1 subunit gene (GABA1) are not associated with idiopathic gonadotropin-dependent precocious puberty in girls with and without eletroencephalographic abnormalites (2005)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: RECEPTORES DE ESTEROIDES; MUTAÇÃO; SISTEMA NERVOSO CENTRAL (RADIOGRAFIA); POLIMORFISMO GENÉTICO; IMAGEM POR RESSONÂNCIA MAGNÉTICA
- Language: Inglês
- Imprenta:
- Publisher: LIM/HC-FMUSP
- Publisher place: São Paulo
- Date published: 2005
- Conference titles: Simpósio Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP
-
ABNT
BRITO, Vinicius Nahime de et al. Allelic variants of the GABA-A receptor alpha-1 subunit gene (GABA1) are not associated with idiopathic gonadotropin-dependent precocious puberty in girls with and without eletroencephalographic abnormalites. 2005, Anais.. São Paulo: LIM/HC-FMUSP, 2005. . Acesso em: 23 abr. 2024. -
APA
Brito, V. N. de, Mendonça, B. B., Guilhoto, L. M. F. F., Freitas, K. C. M., Arnhold, I. J. P., & Latronico, A. C. (2005). Allelic variants of the GABA-A receptor alpha-1 subunit gene (GABA1) are not associated with idiopathic gonadotropin-dependent precocious puberty in girls with and without eletroencephalographic abnormalites. In . São Paulo: LIM/HC-FMUSP. -
NLM
Brito VN de, Mendonça BB, Guilhoto LMFF, Freitas KCM, Arnhold IJP, Latronico AC. Allelic variants of the GABA-A receptor alpha-1 subunit gene (GABA1) are not associated with idiopathic gonadotropin-dependent precocious puberty in girls with and without eletroencephalographic abnormalites. 2005 ;[citado 2024 abr. 23 ] -
Vancouver
Brito VN de, Mendonça BB, Guilhoto LMFF, Freitas KCM, Arnhold IJP, Latronico AC. Allelic variants of the GABA-A receptor alpha-1 subunit gene (GABA1) are not associated with idiopathic gonadotropin-dependent precocious puberty in girls with and without eletroencephalographic abnormalites. 2005 ;[citado 2024 abr. 23 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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