Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty (2011)
- Authors:
- USP affiliated authors: XAVIER, ANA CLAUDIA LATRÔNICO - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidade: FM
- DOI: 10.1530/EJE-11-016
- Subjects: MUTAÇÃO GENÉTICA; GENES (ANÁLISE); PUBERDADE; CRESCIMENTO; RECEPTORES
- Language: Inglês
- Imprenta:
- Source:
- Título: European journal of endocrinology
- ISSN: 0804-4643
- Volume/Número/Paginação/Ano: v. 165, n. 2, p. 233-241, 2011
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
PIRES, Patricia N. Pugliese et al. Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty. European journal of endocrinology, v. 165, n. 2, p. 233-241, 2011Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-016. Acesso em: 28 dez. 2025. -
APA
Pires, P. N. P., Fortin, J. -P., Arthur, T., Xavier, A. C. L., Mendonça, B. B. de, Villares, S. M. F., et al. (2011). Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty. European journal of endocrinology, 165( 2), 233-241. doi:10.1530/EJE-11-016 -
NLM
Pires PNP, Fortin J-P, Arthur T, Xavier ACL, Mendonça BB de, Villares SMF, Arnhold IJP, Kopin AS, Jorge AA de L. Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty [Internet]. European journal of endocrinology. 2011 ; 165( 2): 233-241.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1530/EJE-11-016 -
Vancouver
Pires PNP, Fortin J-P, Arthur T, Xavier ACL, Mendonça BB de, Villares SMF, Arnhold IJP, Kopin AS, Jorge AA de L. Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty [Internet]. European journal of endocrinology. 2011 ; 165( 2): 233-241.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1530/EJE-11-016 - Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay
- Mutational analysis of TAC3 and TACR3 genes in patients with idiopathic central pubertal disorders
- Amplification of the Insulin-Like Growth Factor 1 Receptor Gene Is a Rare Event in Adrenocortical Adenocarcinomas: Searching for Potential Mechanisms of Overexpression
- Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities
- The role of fibroblast growth factor receptor 4 overexpression and gene amplification as prognostic markers in pediatric and adult adrenocortical tumors [Carta]
- Analysis of FGFR4 Locus amplification in pediatric and adult sporadic adrenocortical tumors
- Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty
- Deleterious variants in intolerant genes reveal new candidates for self-limited delayed puberty
- Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line
- Clinical and Genetic Characterization of Familial Central Precocious Puberty
Informações sobre o DOI: 10.1530/EJE-11-016 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
