Article Versions Notes

Van Heurck R, Carminho-Rodrigues MT, Ranza E, Stafuzza C, Quteineh L, Gehrig C, Hammar E, Guipponi M, Abramowicz M, Senn P, et al. Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss. Genes. 2021; 12(8):1277. https://doi.org/10.3390/genes12081277

Van Heurck, Roxane, Maria Teresa Carminho-Rodrigues, Emmanuelle Ranza, Caterina Stafuzza, Lina Quteineh, Corinne Gehrig, Eva Hammar, Michel Guipponi, Marc Abramowicz, Pascal Senn, and et al. 2021. "Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss" Genes 12, no. 8: 1277. https://doi.org/10.3390/genes12081277

Van Heurck, R., Carminho-Rodrigues, M. T., Ranza, E., Stafuzza, C., Quteineh, L., Gehrig, C., Hammar, E., Guipponi, M., Abramowicz, M., Senn, P., Guinand, N., Cao-Van, H., & Paoloni-Giacobino, A. (2021). Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss. Genes, 12(8), 1277. https://doi.org/10.3390/genes12081277