Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect (2002)
- Authors:
- USP affiliated authors: MENDONCA, BERENICE BILHARINHO DE - FM ; ARNHOLD, IVO J. P. - FM ; BACHEGA, TANIA A. S. S. - FM
- Unidade: FM
- Subjects: ENDOCRINOLOGIA; GENÉTICA MOLECULAR
- Language: Inglês
- Imprenta:
- Source:
- Título: The Journal of Clinical Endocrinology & Metabolism
- Volume/Número/Paginação/Ano: v. 87, n. 9, p. 4314-4317, 2002
-
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: 29 dez. 2025. -
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 2025 dez. 29 ] -
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 2025 dez. 29 ] - Reavaliação na idade adulta do diagnóstico da deficiência de GH (DGH) determinado na infância
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