Combined use of karyotyping and copy number variation sequencing technology in prenatal diagnosis

Lignende værker

• Combined use of karyotyping and copy number variation sequencing technology in prenatal diagnosis
  af: Suhua Zhang, et al.
  Udgivet: (2022-12-01)
• Accuracy of expanded noninvasive prenatal testing for maternal copy number variations: A comparative study with CNV-seq of maternal lymphocyte DNA
  af: Honglei Duan, et al.
  Udgivet: (2024-07-01)
• Performance of expanded non-invasive prenatal testing for fetal aneuploidies and copy-number variations in 9,708 pregnancies
  af: Feng Suo, et al.
  Udgivet: (2026-01-01)
• In the era of copy number variation sequencing: changes in the target population for prenatal diagnosis and what is the optimal prenatal diagnostic strategy?
  af: Shaozhe Yang, et al.
  Udgivet: (2025-12-01)
• Prenatal Diagnosis and Pregnancy Outcome Analysis of High-risk Fetuses Suggested by Noninvasive Prenatal Screening
  af: Yan LUO, Bingyi ZHAO, Yanmei SUN, Haishen TIAN, Yali LI, Yanshang ZHANG, Jian GAO, Zhiqiang CUI
  Udgivet: (2022-07-01)