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Baby’s first genome
Nature Biotechnology ( IF 33.1 ) Pub Date : 2022-04-25 , DOI: 10.1038/s41587-022-01306-1
Caroline Seydel 1
Affiliation  

Whole-genome sequencing may be the fastest way to diagnose rare complex diseases, but should it be incorporated into healthy newborn screening?

中文翻译:

婴儿的第一个基因组

全基因组测序可能是诊断罕见复杂疾病的最快方法,但它是否应该纳入健康新生儿筛查?
更新日期:2022-04-26
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