Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: FENÓTIPOS (VARIAÇÃO), HIDROXILASE (DEFICIÊNCIA), DNA (ANÁLISE), GENOMAS
ABNT
ARAÚJO, Rogério S. et al. Microconversion between CYP21A2 and CYP21A1P Promoter Regions Causes the Nonclassical Form of 21-Hydroxylase Deficiency. Journal of Clinical Endocrinology and Metabolism, v. 92, n. 10, p. 4028-4034, 2007Tradução . . Disponível em: https://doi.org/10.1210/jc.2006-2163. Acesso em: 23 ago. 2024.APA
Araújo, R. S., Mendonça, B. B., Barbosa, Â. S., Lin, C. J., Marcondes, J. A. M., Billerbeck, A. E. C., & Bachega, T. A. S. S. (2007). Microconversion between CYP21A2 and CYP21A1P Promoter Regions Causes the Nonclassical Form of 21-Hydroxylase Deficiency. Journal of Clinical Endocrinology and Metabolism, 92( 10), 4028-4034. doi:10.1210/jc.2006-2163NLM
Araújo RS, Mendonça BB, Barbosa ÂS, Lin CJ, Marcondes JAM, Billerbeck AEC, Bachega TASS. Microconversion between CYP21A2 and CYP21A1P Promoter Regions Causes the Nonclassical Form of 21-Hydroxylase Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2007 ; 92( 10): 4028-4034.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1210/jc.2006-2163Vancouver
Araújo RS, Mendonça BB, Barbosa ÂS, Lin CJ, Marcondes JAM, Billerbeck AEC, Bachega TASS. Microconversion between CYP21A2 and CYP21A1P Promoter Regions Causes the Nonclassical Form of 21-Hydroxylase Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2007 ; 92( 10): 4028-4034.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1210/jc.2006-2163