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: 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: 28 dez. 2025. , 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 2025 dez. 28 ] 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 2025 dez. 28 ] Available from: https://doi.org/10.1159/000343182 - Deleterious variants in intolerant genes reveal new candidates for self-limited delayed puberty
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- Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty
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- Aplicação da genética molecular no manejo dos distúrbios do crescimento
- Deficiência da STAT5B: uma nova síndrome de insensibilidade ao hormônio de crescimento associada a acometimento imunológico
Informações sobre o DOI: 10.1159/000343182 (Fonte: oaDOI API)
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