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Expanded Newborn Screening Using Genome Sequencing for Early Actionable Conditions
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Genetic screening for hearing impairment and the genotype-phenotype correlation of GJB2 c.109G>A variants in 47,729 neonates: a population-based study in southern China
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胎儿游离DNA在单基因遗传病检测的研究进展
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胎儿游离DNA在单基因遗传病检测的研究进展
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新一代无创产前筛查技术NIPT2.0临床应用策略专家共识
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