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)
- Autores:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Assuntos: RECEPTORES DE ESTEROIDES; MUTAÇÃO; SISTEMA NERVOSO CENTRAL (RADIOGRAFIA); POLIMORFISMO GENÉTICO; IMAGEM POR RESSONÂNCIA MAGNÉTICA
- Idioma: Inglês
- Imprenta:
- Editora: LIM/HC-FMUSP
- Local: São Paulo
- Data de publicação: 2005
- Nome do evento: 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
- Absense of duplication on DAX1 gene in patients with 46,XY sex reversal
- Crescimento linear e estatura final em crianças com tumores adrenais predominantemente virilizantes
- Absense of inactivating mutations and deletions of DAX1 gene in SRY negative 46,XX sex-reversed patients
- Heterogeneidade clínica e molecular do hipogonadismo hipogonadotrófico (HH): importância da avaliação do sistema olfatório no diagnóstico diferencial
- Number of CAG repeats in Exon 1 of androgen receptor gene is not related to gender identity in adult patients with male psudohermaphroditism and male transexualism
- Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitibity syndrome in a brazilian cohort: five novel mutations in the androgen receptor gene
- Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
- Reavaliação na idade adulta do diagnóstico da deficiência de GH (DGH) determinado na infância
- Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty
Como citar
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
