Correlation between degree of external genitalia virilization and CAG repeats of the androgen receptor gene in DNA sample of peripheral leukocytes and pubic hair of women with 21-hydroxylase deficiency (2007)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: DNA; ENZIMAS (DEFICIÊNCIA); HIDROXILASE (DEFICIÊNCIA); LEUCÓCITOS; RESUMOS (SIMPÓSIOS)
- Language: Inglês
- Imprenta:
- Source:
- Conference titles: Simpósio avanços em pesquisas médicas
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ABNT
KAUPERT, L. C. et al. Correlation between degree of external genitalia virilization and CAG repeats of the androgen receptor gene in DNA sample of peripheral leukocytes and pubic hair of women with 21-hydroxylase deficiency. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 abr. 2024. , 2007 -
APA
Kaupert, L. C., Billerbeck, A. E. C., Brito, V. N., Mendonça, B. B. de, & Bachega, T. A. S. S. (2007). Correlation between degree of external genitalia virilization and CAG repeats of the androgen receptor gene in DNA sample of peripheral leukocytes and pubic hair of women with 21-hydroxylase deficiency. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Kaupert LC, Billerbeck AEC, Brito VN, Mendonça BB de, Bachega TASS. Correlation between degree of external genitalia virilization and CAG repeats of the androgen receptor gene in DNA sample of peripheral leukocytes and pubic hair of women with 21-hydroxylase deficiency. Clinics. 2007 ; 62 S82.[citado 2024 abr. 24 ] -
Vancouver
Kaupert LC, Billerbeck AEC, Brito VN, Mendonça BB de, Bachega TASS. Correlation between degree of external genitalia virilization and CAG repeats of the androgen receptor gene in DNA sample of peripheral leukocytes and pubic hair of women with 21-hydroxylase deficiency. Clinics. 2007 ; 62 S82.[citado 2024 abr. 24 ] - Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
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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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