Bengl, D., Koparir, A., Prastyo, W. E., Remmele, C., Dittrich, M., Flandin, S., . . . Hofrichter, M. A. H. Whole-genome sequencing, as a powerful diagnostic tool in hearing loss, reveals novel variants in PTPRQ missed by whole-exome sequencing. BMC.
Chicago Style (17th ed.) CitationBengl, Daniel, et al. Whole-genome Sequencing, as a Powerful Diagnostic Tool in Hearing Loss, Reveals Novel Variants in PTPRQ Missed by Whole-exome Sequencing. BMC.
MLA (9th ed.) CitationBengl, Daniel, et al. Whole-genome Sequencing, as a Powerful Diagnostic Tool in Hearing Loss, Reveals Novel Variants in PTPRQ Missed by Whole-exome Sequencing. BMC.
Warning: These citations may not always be 100% accurate.