Source: Journal of pediatric endocrinology and metabolism. Conference titles: Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP). Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, BIOLOGIA MOLECULAR, HIDROXILASE (DEFICIÊNCIA), GENÓTIPOS, POLIMORFISMO, RESUMOS (CONGRESSOS)
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ARAUJO, R. S. et al. Microconversion between pseudogene and CYP21A2 reduces the transcriptional activity causing nonclassical form of 21-hydroxylase deficiency. Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2004APA
Araujo, R. S., Barbosa, A. S., Mendonça, B. B., Lin, C. J., Billerbeck, C. J., Marcondes, J. A. M., & Bachega, T. A. S. S. (2004). Microconversion between pseudogene and CYP21A2 reduces the transcriptional activity causing nonclassical form of 21-hydroxylase deficiency. Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo.NLM
Araujo RS, Barbosa AS, Mendonça BB, Lin CJ, Billerbeck CJ, Marcondes JAM, Bachega TASS. Microconversion between pseudogene and CYP21A2 reduces the transcriptional activity causing nonclassical form of 21-hydroxylase deficiency. Journal of pediatric endocrinology and metabolism. 2004 ; 17( suppl.5): 1334.[citado 2024 nov. 05 ]Vancouver
Araujo RS, Barbosa AS, Mendonça BB, Lin CJ, Billerbeck CJ, Marcondes JAM, Bachega TASS. Microconversion between pseudogene and CYP21A2 reduces the transcriptional activity causing nonclassical form of 21-hydroxylase deficiency. Journal of pediatric endocrinology and metabolism. 2004 ; 17( suppl.5): 1334.[citado 2024 nov. 05 ]
