Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty (2012)
- Authors:
- USP affiliated authors: XAVIER, ANA CLAUDIA LATRÔNICO - FM ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidade: FM
- DOI: 10.1159/000343182
- Subjects: HIPOGONADISMO (DIAGNÓSTICO); GENES; CRESCIMENTO (DEFICIÊNCIA); FENÓTIPOS; POLIMORFISMO; DOENÇAS GENÉTICAS (DIAGNÓSTICO); RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Hormone research in paediatrics
- ISSN: 0301-0163
- Volume/Número/Paginação/Ano: v.78, n. suppl. 1,res. P1-d3-378, p. 119, 2012
- Conference titles: 51th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE)
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
SILVEIRA, Leticia F. G. et al. Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000343182. Acesso em: 26 abr. 2024. , 2012 -
APA
Silveira, L. F. G., Tusset, C., Moura, L., Beneduzzi, D., Teles, M., Jorge, A. A. L., et al. (2012). Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000343182 -
NLM
Silveira LFG, Tusset C, Moura L, Beneduzzi D, Teles M, Jorge AAL, Trarbach EB, Latronico AC. Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty [Internet]. Hormone research in paediatrics. 2012 ;78( suppl. 1): 119.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1159/000343182 -
Vancouver
Silveira LFG, Tusset C, Moura L, Beneduzzi D, Teles M, Jorge AAL, Trarbach EB, Latronico AC. Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty [Internet]. Hormone research in paediatrics. 2012 ;78( suppl. 1): 119.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1159/000343182 - Mutational analysis of TAC3 and TACR3 genes in patients with idiopathic central pubertal disorders
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- Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities
- Clinical and Genetic Characterization of Familial Central Precocious Puberty
- Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line
- Genetics basis for GnRH-dependent pubertal disorders in humans
Informações sobre o DOI: 10.1159/000343182 (Fonte: oaDOI API)
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