Cite
Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective.
MLA
Félix, Têmis Maria, et al. “Challenges and Recommendations to Increasing the Use of Exome Sequencing and Whole Genome Sequencing for Diagnosing Rare Diseases in Brazil: An Expert Perspective.” International Journal for Equity in Health, vol. 22, no. 1, Jan. 2023, pp. 1–10. EBSCOhost, https://doi.org/10.1186/s12939-022-01809-y.
APA
Félix, T. M., Fischinger Moura de Souza, C., Oliveira, J. B., Rico-Restrepo, M., Zanoteli, E., Zatz, M., & Giugliani, R. (2023). Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective. International Journal for Equity in Health, 22(1), 1–10. https://doi.org/10.1186/s12939-022-01809-y
Chicago
Félix, Têmis Maria, Carolina Fischinger Moura de Souza, João Bosco Oliveira, Mariana Rico-Restrepo, Edmar Zanoteli, Mayana Zatz, and Roberto Giugliani. 2023. “Challenges and Recommendations to Increasing the Use of Exome Sequencing and Whole Genome Sequencing for Diagnosing Rare Diseases in Brazil: An Expert Perspective.” International Journal for Equity in Health 22 (1): 1–10. doi:10.1186/s12939-022-01809-y.