Félix, Têmis Maria 
; Souza, Carolina Fischinger Moura de ; Oliveira, João Bosco; Rico-Restrepo, Mariana; Zanoteli, Edmar ; Zatz, Mayana ; Giugliani, Roberto
Source: International Journal for Equity in Health. Unidades: IB, FM
Subjects: GENOMAS, SEQUENCIAMENTO GENÉTICO, DOENÇAS RARAS
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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, v. 22, n. 11, 2023Tradução . . Disponível em: https://doi.org/10.1186/s12939-022-01809-y. Acesso em: 15 nov. 2024.APA
Félix, T. M., Souza, C. F. M. de, 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( 11). doi:10.1186/s12939-022-01809-yNLM
Félix TM, Souza CFM de, Oliveira JB, Rico-Restrepo M, Zanoteli E, Zatz M, Giugliani R. Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective [Internet]. International Journal for Equity in Health. 2023 ;22( 11):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/s12939-022-01809-yVancouver
Félix TM, Souza CFM de, Oliveira JB, Rico-Restrepo M, Zanoteli E, Zatz M, Giugliani R. Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective [Internet]. International Journal for Equity in Health. 2023 ;22( 11):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/s12939-022-01809-y
