Subjects: HIDROXILASE (DEFICIÊNCIA), GENÉTICA, ESTUDOS RETROSPECTIVOS, HIPERPLASIAS (DIAGNÓSTICO), RADIOIMUNOENSAIO
ABNT
GOMES, Larissa G. et al. Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics, v. 68, n. 2, p. 147-151, 2013Tradução . . Disponível em: https://doi.org/10.6061/CLINICS/2013(02)OA05. Acesso em: 18 fev. 2026.APA
Gomes, L. G., Madureira, G., Mendonca, B. B., & Bachega, T. A. S. S. (2013). Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics, 68( 2), 147-151. doi:10.6061/CLINICS/2013(02)OA05NLM
Gomes LG, Madureira G, Mendonca BB, Bachega TASS. Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency [Internet]. Clinics. 2013 ; 68( 2): 147-151.[citado 2026 fev. 18 ] Available from: https://doi.org/10.6061/CLINICS/2013(02)OA05Vancouver
Gomes LG, Madureira G, Mendonca BB, Bachega TASS. Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency [Internet]. Clinics. 2013 ; 68( 2): 147-151.[citado 2026 fev. 18 ] Available from: https://doi.org/10.6061/CLINICS/2013(02)OA05
