Source: Archives of endocrinology metabolism. Unidade: FM
Subjects: HIPERPLASIA SUPRARRENAL CONGÊNITA, HORMÔNIO DO CRESCIMENTO, DOENÇAS DO DESENVOLVIMENTO ÓSSEO
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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:10.1590/2359-3997000000311NLM
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/10.1590/2359-3997000000311Vancouver
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
