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A capture-based method of prenatal cell-free DNA screening for autosomal recessive non-syndromic hearing loss.

Qian MuLing BaiBing XuHuawen DuZhaoyun JiangShasha HuangBo GaoQixi WuHanqing ZhaoPu DaiYi Jiang
Published in: Prenatal diagnosis (2024)
This capture-based method of prenatal screening by cfDNA demonstrated strong potential for fetal genotyping of autosomal recessive disorders.
Keyphrases
  • intellectual disability
  • pregnant women
  • hearing loss
  • muscular dystrophy
  • autism spectrum disorder
  • high throughput
  • genome wide
  • gene expression
  • dna methylation
  • human health