An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm

The second Newborn Sequencing in Genomic Medicine and Public Health (NSIGHT2) study was a randomized, controlled trial of rapid whole-genome sequencing (rWGS) or rapid whole-exome sequencing (rWES) in infants with diseases of unknown etiology in intensive care units (ICUs). Gravely ill infants were...

全面介紹

Na minha lista:
書目詳細資料
發表在:Am J Hum Genet
Main Authors: Dimmock, David P., Clark, Michelle M., Gaughran, Mary, Cakici, Julie A., Caylor, Sara A., Clarke, Christina, Feddock, Michele, Chowdhury, Shimul, Salz, Lisa, Cheung, Cynthia, Bird, Lynne M., Hobbs, Charlotte, Wigby, Kristen, Farnaes, Lauge, Bloss, Cinnamon S., Kingsmore, Stephen F.
格式: Artigo
語言:Inglês
出版: Elsevier 2020
主題:
Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC7675004/
https://ncbi.nlm.nih.gov/pubmed/33157007
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2020.10.003
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!

相似書籍