Source: Hormone research. Conference titles: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Subjects: TÉCNICAS DE DIAGNÓSTICO E PROCEDIMENTOS, MUTAÇÃO GENÉTICA (ETIOLOGIA), POLIMORFISMO
ABNT
GOMES, C. et al. TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development. Hormone research, v. 68, p. 12, 2007Tradução . . Acesso em: 28 set. 2024.APA
Gomes, C., Domenice, S., Santos, M., Arnhold, I., Mendonça, B. B. de, & Costa, E. (2007). TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development. Hormone research, 68, 12.NLM
Gomes C, Domenice S, Santos M, Arnhold I, Mendonça BB de, Costa E. TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development. Hormone research. 2007 ; 68 12.[citado 2024 set. 28 ]Vancouver
Gomes C, Domenice S, Santos M, Arnhold I, Mendonça BB de, Costa E. TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development. Hormone research. 2007 ; 68 12.[citado 2024 set. 28 ]