Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing (2017)
- Authors:
- USP affiliated authors: BACHEGA, TÂNIA APARECIDA SARTORI SANCHEZ - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidade: FM
- DOI: 10.1590/2359-3997000000311
- Subjects: HIPERPLASIA SUPRARRENAL CONGÊNITA; HORMÔNIO DO CRESCIMENTO; DOENÇAS DO DESENVOLVIMENTO ÓSSEO
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Rio de Janeiro, Rj
- Date published: 2017
- Source:
- Título: Archives of endocrinology metabolism
- ISSN: 2359-3997
- Volume/Número/Paginação/Ano: v. 61, n. 6, p. 633-636, 2017
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
CORREA, Fernanda A. et al. Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing. Archives of endocrinology metabolism, v. 61, n. 6, p. 633-636, 2017Tradução . . Disponível em: https://doi.org/10.1590/2359-3997000000311. Acesso em: 22 jan. 2026. -
APA
Correa, F. A., França, M. M., Fang, Q., Ma, Q., Bachega, T. A. S. S., Rodrigues, A., et al. (2017). Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing. Archives of endocrinology metabolism, 61( 6), 633-636. doi:10.1590/2359-3997000000311 -
NLM
Correa FA, França MM, Fang Q, Ma Q, Bachega TASS, Rodrigues A, Ozel BA, Li JZ, Mendonça BB de, Jorge AA de L, Carvalho LR, Camper SA, Arnhold IJ. Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing [Internet]. Archives of endocrinology metabolism. 2017 ; 61( 6): 633-636.[citado 2026 jan. 22 ] Available from: https://doi.org/10.1590/2359-3997000000311 -
Vancouver
Correa FA, França MM, Fang Q, Ma Q, Bachega TASS, Rodrigues A, Ozel BA, Li JZ, Mendonça BB de, Jorge AA de L, Carvalho LR, Camper SA, Arnhold IJ. Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing [Internet]. Archives of endocrinology metabolism. 2017 ; 61( 6): 633-636.[citado 2026 jan. 22 ] Available from: https://doi.org/10.1590/2359-3997000000311 - Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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Informações sobre o DOI: 10.1590/2359-3997000000311 (Fonte: oaDOI API)
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