Source: European Journal of Medical Genetics. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, GENES, TRANSTORNOS GONADAIS, TESTÍCULO (CRESCIMENTO E DESENVOLVIMENTO)
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MACHADO, Aline Zamboni et al. Absence of inactivating mutations and deletions in the DMRT1 and FGF9 genes in a large cohort of 46,XY patients with gonadal dysgenesis. European Journal of Medical Genetics, v. 55, n. 12, p. 690-694, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2012.07.012. Acesso em: 19 out. 2024.APA
Machado, A. Z., Silva, T. E. da, Costa, E. M. F., Santos, M. G. dos, Nishi, M. Y., Brito, V. N., et al. (2012). Absence of inactivating mutations and deletions in the DMRT1 and FGF9 genes in a large cohort of 46,XY patients with gonadal dysgenesis. European Journal of Medical Genetics, 55( 12), 690-694. doi:10.1016/j.ejmg.2012.07.012NLM
Machado AZ, Silva TE da, Costa EMF, Santos MG dos, Nishi MY, Brito VN, Mendonca BB, Domenice S. Absence of inactivating mutations and deletions in the DMRT1 and FGF9 genes in a large cohort of 46,XY patients with gonadal dysgenesis [Internet]. European Journal of Medical Genetics. 2012 ; 55( 12): 690-694.[citado 2024 out. 19 ] Available from: https://doi.org/10.1016/j.ejmg.2012.07.012Vancouver
Machado AZ, Silva TE da, Costa EMF, Santos MG dos, Nishi MY, Brito VN, Mendonca BB, Domenice S. Absence of inactivating mutations and deletions in the DMRT1 and FGF9 genes in a large cohort of 46,XY patients with gonadal dysgenesis [Internet]. European Journal of Medical Genetics. 2012 ; 55( 12): 690-694.[citado 2024 out. 19 ] Available from: https://doi.org/10.1016/j.ejmg.2012.07.012