Genetic analysis of thyroid transcription factor1 (TTF-1) gene in patients with central pubertal disorders (2008)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; XAVIER, ANA CLAUDIA LATRÔNICO - FM
- Unidade: FM
- Subjects: DNA (EXTRAÇÃO); RATOS; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Arquivos Brasileiros de Endocrinologia e Metabologia
- ISSN: 0004-2730
- Volume/Número/Paginação/Ano: v. 52, supl. 6, parte II, p. S796, res. OP-102, 2008
- Conference titles: International Congress of Endocrinology
-
ABNT
CUKIER, P. et al. Genetic analysis of thyroid transcription factor1 (TTF-1) gene in patients with central pubertal disorders. Arquivos Brasileiros de Endocrinologia e Metabologia. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 fev. 2026. , 2008 -
APA
Cukier, P., Brito, V. N., Latronico, A. C., & Mendonça, B. B. (2008). Genetic analysis of thyroid transcription factor1 (TTF-1) gene in patients with central pubertal disorders. Arquivos Brasileiros de Endocrinologia e Metabologia. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Cukier P, Brito VN, Latronico AC, Mendonça BB. Genetic analysis of thyroid transcription factor1 (TTF-1) gene in patients with central pubertal disorders. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52 S796.[citado 2026 fev. 04 ] -
Vancouver
Cukier P, Brito VN, Latronico AC, Mendonça BB. Genetic analysis of thyroid transcription factor1 (TTF-1) gene in patients with central pubertal disorders. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52 S796.[citado 2026 fev. 04 ] - Fatores determinantes da estatura final normal em meninas com puberdade precoce dependente de gonadotrofinas tratadas com análogos de GnRII depot
- Análise dos valares de LH 2 horas após acetato de leuprolide depot na monitorização do tratamento da puberdade precoce dependente de gonadotrofinas
- Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD)
- Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction
- XAF1 as a modifier of p53 function and cancer susceptibility
- Localization of Occult Adrenal Tissue with Cosyntropin-Stimulated 18F-FDG-PET/CT in a Patient with Metachronous Adrenocortical Tumor Who Presented with Persistently Elevated DHEAS after Bilateral Adrenalectomy
- A novel missense variant in the Necdin gene in a male patient with kallmann syndrome
- Molecular analysis of the neuropeptide Y1 receptor gene in human idiopathic gonadotropin-dependent precocious puberty and isolated hypogonadotropic hypogonadism
- Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty
- Long-term outcomes of Patients with Central Precocious Puberty due to Hypothalamic Hamartoma after GnRHa Treatment: anthropometric, Metabolic, and Reproductive Aspects
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
