Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Subjects: ENDOCRINOLOGIA, METABOLISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BACHEGA, Tania A. S. S. et al. Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 16 maio 2024. , 2001APA
Bachega, T. A. S. S., Billerbeck, A. E. C., Madureira, G., Marcondes, J. A. M., Pinto, E. M., Correa, R. P., et al. (2001). Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.NLM
Bachega TASS, Billerbeck AEC, Madureira G, Marcondes JAM, Pinto EM, Correa RP, Arnhold IJP, Mendonca BB. Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations. Pediatric Research. 2001 ; 49( 4 pt. 2): 113A. res. PI-670.[citado 2024 maio 16 ]Vancouver
Bachega TASS, Billerbeck AEC, Madureira G, Marcondes JAM, Pinto EM, Correa RP, Arnhold IJP, Mendonca BB. Molecular study of 181 brazilian patients with 21-hydroxylase deficiency: identification of six new mutations. Pediatric Research. 2001 ; 49( 4 pt. 2): 113A. res. PI-670.[citado 2024 maio 16 ]