Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: HORMÔNIOS SEXUAIS FEMININOS (DEFICIÊNCIA), GENITÁLIA FEMININA (ANORMALIDADES), ATIVAÇÃO ENZIMÁTICA, RECEPTORES ANDROGÊNICOS (GENÉTICA)
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ROCHA, R. et al. Study of CAG repeat in the exon 1 of the androgen receptor gene in 106 female patients with the classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 15 maio 2024.APA
Rocha, R., Billerbeck, a. E., Pinto, E., Melo, K. F., Lin, C. J., Mendonca, B. B., & Bachega, T. A. S. (2004). Study of CAG repeat in the exon 1 of the androgen receptor gene in 106 female patients with the classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. In Program and Abstracts. Lisboa: International Society of Endocrinology.NLM
Rocha R, Billerbeck a. E, Pinto E, Melo KF, Lin CJ, Mendonca BB, Bachega TAS. Study of CAG repeat in the exon 1 of the androgen receptor gene in 106 female patients with the classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Program and Abstracts. 2004 ;[citado 2024 maio 15 ]Vancouver
Rocha R, Billerbeck a. E, Pinto E, Melo KF, Lin CJ, Mendonca BB, Bachega TAS. Study of CAG repeat in the exon 1 of the androgen receptor gene in 106 female patients with the classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Program and Abstracts. 2004 ;[citado 2024 maio 15 ]