Applications of Noninvasive Prenatal Testing for Subchromosomal Copy Number Variations Using Cell-Free DNA

Clin Lab Med. 2022 Dec;42(4):613-625. doi: 10.1016/j.cll.2022.09.014.

Authors

Jiale Xiang¹, Zhiyu Peng²

Affiliations

¹ BGI Genomics, BGI-Shenzhen, Shenzhen 518083, China; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
² BGI Genomics, BGI-Shenzhen, Shenzhen 518083, China; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China. Electronic address: pengzhiyu@bgi.com.

PMID: 36368786
DOI: 10.1016/j.cll.2022.09.014

No abstract available

Keywords: Copy number variation; Microdeletion; Microduplication; Noninvasive prenatal testing; Prenatal screening; Subchromosomal abnormalities.

Publication types

Review

MeSH terms

Aneuploidy
Cell-Free Nucleic Acids*
Chromosome Disorders*
DNA Copy Number Variations
Female
Humans
Noninvasive Prenatal Testing*
Pregnancy
Prenatal Diagnosis

Substances

Cell-Free Nucleic Acids