Mutational analysis of LIN28B gene in children with idiopathic central precocious puberty (2010)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; XAVIER, ANA CLAUDIA LATRÔNICO - FM
- Unidade: FM
- Subjects: CRIANÇAS; PUBERDADE PRECOCE (GENÉTICA); MUTAÇÃO GENÉTICA; GENES (ANÁLISE); POLIMORFISMO; GENOMAS; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Hormone Research in Paediatrics
- ISSN: 1663-2818
- Volume/Número/Paginação/Ano: v. 74, n. suppl. 3, p. 45, res. FC13-151, 2010
- Conference titles: Annual meeting of the European Society for Pediatric Endocrinology (ESPE)
-
ABNT
SILVEIRA-NETO, Acacio et al. Mutational analysis of LIN28B gene in children with idiopathic central precocious puberty. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 abr. 2024. , 2010 -
APA
Silveira-Neto, A., Silveira, L. G., Beneduzzi, D., Brito, V. N., Cukier, P., Arnhold, I. J., et al. (2010). Mutational analysis of LIN28B gene in children with idiopathic central precocious puberty. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Silveira-Neto A, Silveira LG, Beneduzzi D, Brito VN, Cukier P, Arnhold IJ, Mendonca BB, Latronico AC. Mutational analysis of LIN28B gene in children with idiopathic central precocious puberty. Hormone Research in Paediatrics. 2010 ; 74( suppl. 3): 45.[citado 2024 abr. 24 ] -
Vancouver
Silveira-Neto A, Silveira LG, Beneduzzi D, Brito VN, Cukier P, Arnhold IJ, Mendonca BB, Latronico AC. Mutational analysis of LIN28B gene in children with idiopathic central precocious puberty. Hormone Research in Paediatrics. 2010 ; 74( suppl. 3): 45.[citado 2024 abr. 24 ] - Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life
- Puberdade precoce central
- Methylome profiling of healthy and central precocious puberty girls
- Clinical and molecular aspects of a pediatric metachronous adrenocortical tumor
- Mutational analysis of LIN28BGENE in children with idiopathic central precocious puberty
- Effectiveness of leuprolide acetate 3-month depot (11.25 mg) in the treatment of patients with central precocious puberty: experience of
- Phenotype-genotype correlations in patients with inactivating gonadotropin hormone receptor mutations
- Molecular analysis of the neuropeptide Y1 receptor gene in human idiopathic gonadotropin-dependent precocious puberty and isolated hypogonadotropic hypogonadism
- 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
- Fatores determinantes da estatura final normal em meninas com puberdade precoce dependente de gonadotrofinas tratadas com análogos de GnRII depot
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
