Source: Hormone Research in Paediatrics. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, TRANSTORNOS GONADAIS, CROMOSSOMOS SEXUAIS (FISIOPATOLOGIA)
ABNT
NISHI, Mirian Yumie et al. The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants. Hormone Research in Paediatrics, v. 75, n. 1, p. 26-31, 2011Tradução . . Disponível em: https://doi.org/10.1159/000316536. Acesso em: 19 out. 2024.APA
Nishi, M. Y., Costa, E. M. F., Oliveira, S. B., Mendonca, B. B., & Domenice, S. (2011). The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants. Hormone Research in Paediatrics, 75( 1), 26-31. doi:10.1159/000316536NLM
Nishi MY, Costa EMF, Oliveira SB, Mendonca BB, Domenice S. The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants [Internet]. Hormone Research in Paediatrics. 2011 ; 75( 1): 26-31.[citado 2024 out. 19 ] Available from: https://doi.org/10.1159/000316536Vancouver
Nishi MY, Costa EMF, Oliveira SB, Mendonca BB, Domenice S. The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants [Internet]. Hormone Research in Paediatrics. 2011 ; 75( 1): 26-31.[citado 2024 out. 19 ] Available from: https://doi.org/10.1159/000316536