21-hydroxylase deficiency (classic form) in black descendents from Bahia: molecular, clinical and familial study (2001)
- Authors:
- Autor USP: MENDONCA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: ENDOCRINOLOGIA; MOLÉCULA
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2001
- Source:
- Título do periódico: Pediatric Research
- ISSN: 0031-3998
- Volume/Número/Paginação/Ano: v. 49, n. 4 pt. 2, p. 113A. res. PI-673, 2001
- Conference titles: Annual Meeting of the Pediatric Academic Societies
-
ABNT
TORALLES, Maria Betania M. B. et al. 21-hydroxylase deficiency (classic form) in black descendents from Bahia: molecular, clinical and familial study. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 16 maio 2024. , 2001 -
APA
Toralles, M. B. M. B., Billerbeck, A. E. C., Mendonca, B. B., & Azevedo, E. (2001). 21-hydroxylase deficiency (classic form) in black descendents from Bahia: molecular, clinical and familial study. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Toralles MBMB, Billerbeck AEC, Mendonca BB, Azevedo E. 21-hydroxylase deficiency (classic form) in black descendents from Bahia: molecular, clinical and familial study. Pediatric Research. 2001 ; 49( 4 pt. 2): 113A. res. PI-673.[citado 2024 maio 16 ] -
Vancouver
Toralles MBMB, Billerbeck AEC, Mendonca BB, Azevedo E. 21-hydroxylase deficiency (classic form) in black descendents from Bahia: molecular, clinical and familial study. Pediatric Research. 2001 ; 49( 4 pt. 2): 113A. res. PI-673.[citado 2024 maio 16 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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