Molecular genetics of 21-hydroxylase deficiency in Brazil (1998)
Conference titles: The Endocrinology society Annual Meeting. Unidade: FMAssunto: ENDOCRINOLOGIA PEDIÁTRICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WITCHEL, S.F. et al. Molecular genetics of 21-hydroxylase deficiency in Brazil. 1998, Anais.. New Orleans : Louisiana, 1998: The Endocrinology Society Annual Meeting , 80, 1998. . Acesso em: 18 nov. 2024.APA
Witchel, S. F., Setian, N., Dichtchekenian, V., Crivellaro, C., Smith, R., & Damiani, D. (1998). Molecular genetics of 21-hydroxylase deficiency in Brazil. In . New Orleans : Louisiana, 1998: The Endocrinology Society Annual Meeting , 80.NLM
Witchel SF, Setian N, Dichtchekenian V, Crivellaro C, Smith R, Damiani D. Molecular genetics of 21-hydroxylase deficiency in Brazil. 1998 ;[citado 2024 nov. 18 ]Vancouver
Witchel SF, Setian N, Dichtchekenian V, Crivellaro C, Smith R, Damiani D. Molecular genetics of 21-hydroxylase deficiency in Brazil. 1998 ;[citado 2024 nov. 18 ]