Assessment of diagnostic yield and clinical utility of genome sequencing in critically ill infants.
Moreno CA, de França M, Prota JRM, Migliavacca MP, Teixeira ACB, de Azevedo BMC, de Santana LS, Perrone E, Espolaor JGA, Virmond LA, Minillo RM, Yamada RY, Cintra VP, Quaio CRDC, Ceroni JRM, Chen K, Silva TYT, Coelho AVC, de Oliveira GS, Nascimento Junior JB, Moura LMS, Mofatto LS, Caraciolo MP, Guedes RLM, Barreiro RAS, Gomes CS, Rodrigues RF, Correia LR, Oliveira APA, Carlos CD, da Matta MC, Lima MM, Zurro NB, Ferreira AFM, Colichio GBC, Campilongo GP, da Silva RMR, Ferreira LT, Higaki PI, Pelegrino KO, de Oliveira AC, Micheletti C, Fock RA, Sobreira ACXM, Dos Santos AS, da Silva RTB, Filho JS, Laurentino MBAL, Lyra PT, Cunha ALG, Mendes CCM, Lima JS, Steiner CE, Cavalcanti DP, Heleno JL, Kim CA, Carneiro-Sampaio MMS, de Carvalho WB, Ramos ES, de Almeida ML, Ferriani MPL, de Almeida TF, Oliveira JB.
Moreno CA, et al. Among authors: chen k.
Pediatr Res. 2026 May 8. doi: 10.1038/s41390-026-04861-4. Online ahead of print.
Pediatr Res. 2026.
PMID: 42104137
