A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases
用于新生儿普遍筛查、诊断和严重遗传病精准医疗的基因组测序系统
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2022.08.003
Stephen F Kingsmore, Laurie D Smith, Chris M Kunard, Matthew Bainbridge, Sergey Batalov, Wendy Benson, Eric Blincow, Sara Caylor, Christina Chambers, Guillermo Del Angel, David P Dimmock, Yan Ding, Katarzyna Ellsworth, Annette Feigenbaum, Erwin Frise, Robert C Green, Lucia Guidugli, Kevin P Hall, Ch