Genotype and phenotype of 25 brazilian subjects with androgen insensitivity syndrome (ais) (2003)
- Authors:
- USP affiliated authors: MENDONCA, BERENICE BILHARINHO DE - FM ; ARNHOLD, IVO JORGE PRADO - FM
- Unidade: FM
- Subjects: CLÍNICA GERAL; ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Hormone Research
- Volume/Número/Paginação/Ano: v. 60, n. 3, p. 88, P1-316, 2003
-
ABNT
MELO, K. F. S. et al. Genotype and phenotype of 25 brazilian subjects with androgen insensitivity syndrome (ais). Hormone Research. Baseal: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 abr. 2024. , 2003 -
APA
Melo, K. F. S., Mendonça, B. B., Billerbeck, A. E. C., Costa, E. M. F., Leal, A. M. O., Latronico, A. C., & Arnhold, I. J. P. (2003). Genotype and phenotype of 25 brazilian subjects with androgen insensitivity syndrome (ais). Hormone Research. Baseal: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Melo KFS, Mendonça BB, Billerbeck AEC, Costa EMF, Leal AMO, Latronico AC, Arnhold IJP. Genotype and phenotype of 25 brazilian subjects with androgen insensitivity syndrome (ais). Hormone Research. 2003 ; 60( 3): 88.[citado 2024 abr. 24 ] -
Vancouver
Melo KFS, Mendonça BB, Billerbeck AEC, Costa EMF, Leal AMO, Latronico AC, Arnhold IJP. Genotype and phenotype of 25 brazilian subjects with androgen insensitivity syndrome (ais). Hormone Research. 2003 ; 60( 3): 88.[citado 2024 abr. 24 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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- Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect
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