Fonte: Molecular Cytogenetics. Unidade: FMRP
Assuntos: CROMOSSOMOS SEXUAIS, FENÓTIPOS, INFERTILIDADE MASCULINA, ESPERMATOGÊNESE, CITOGENÉTICA
ABNT
GRZESIUK, Juliana Dourado et al. Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism. Molecular Cytogenetics, v. 9, 2016Tradução . . Disponível em: https://doi.org/10.1186/s13039-016-0249-5. Acesso em: 01 nov. 2024.APA
Grzesiuk, J. D., Pereira, C. S., Grangeiro, C. H. P., Picanço-Albuquerque, C. G., Oliveira-Gennaro, F. G., Machado, F. B., et al. (2016). Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism. Molecular Cytogenetics, 9. doi:10.1186/s13039-016-0249-5NLM
Grzesiuk JD, Pereira CS, Grangeiro CHP, Picanço-Albuquerque CG, Oliveira-Gennaro FG, Machado FB, Medina-Acosta E, Ramos ES, Yoshimoto M, Martelli LR. Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism [Internet]. Molecular Cytogenetics. 2016 ; 9[citado 2024 nov. 01 ] Available from: https://doi.org/10.1186/s13039-016-0249-5Vancouver
Grzesiuk JD, Pereira CS, Grangeiro CHP, Picanço-Albuquerque CG, Oliveira-Gennaro FG, Machado FB, Medina-Acosta E, Ramos ES, Yoshimoto M, Martelli LR. Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism [Internet]. Molecular Cytogenetics. 2016 ; 9[citado 2024 nov. 01 ] Available from: https://doi.org/10.1186/s13039-016-0249-5