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 é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
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: 04 nov. 2024. -
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 2024 nov. 04 ] 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 2024 nov. 04 ] Available from: https://doi.org/10.1590/2359-3997000000311 - Frequency of genetic polymorphisms of PXR gene in the Brazilian population
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Informações sobre o DOI: 10.1590/2359-3997000000311 (Fonte: oaDOI API)
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