Source: The Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Subjects: ENDOCRINOLOGIA, GENÉTICA MOLECULAR
ABNT
BILLERBECK, Ana Elisa C. et al. Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect. The Journal of Clinical Endocrinology & Metabolism, v. 87, n. 9, p. 4314-4317, 2002Tradução . . Acesso em: 26 ago. 2024.APA
Billerbeck, A. E. C., Mendonça, B. B., Pinto, E. M., Madureira, G., Arnhold, I. J. P., & Bachega, T. A. S. S. (2002). Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect. The Journal of Clinical Endocrinology & Metabolism, 87( 9), 4314-4317.NLM
Billerbeck AEC, Mendonça BB, Pinto EM, Madureira G, Arnhold IJP, Bachega TASS. Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect. The Journal of Clinical Endocrinology & Metabolism. 2002 ; 87( 9): 4314-4317.[citado 2024 ago. 26 ]Vancouver
Billerbeck AEC, Mendonça BB, Pinto EM, Madureira G, Arnhold IJP, Bachega TASS. Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect. The Journal of Clinical Endocrinology & Metabolism. 2002 ; 87( 9): 4314-4317.[citado 2024 ago. 26 ]