Analysis of potential copy-number variations and genes associated with first-trimester missed abortion

Analysis of potential copy-number variations and genes associated with first-trimester missed abortion

Background: Copy number variation sequencing (CNV-seq) was proven to be a highly effective tool in studying of chromosomal copy number variations (CNVs) in prenatal diagnosis and post-natal cases with developmental abnormalities. However, the overall characteristics of missed abortion (MA) CNVs were...

Full description

Bibliographic Details
Main Authors: Wen Zeng, Hong Qi, Yang Du, Lirong Cai, Xiaohui Wen, Qian Wan, Yao Luo, Jianjiang Zhu
Format: Article
Language:English
Published: Elsevier 2023-08-01
Series:Heliyon
Subjects:
Copy number variation sequencing
Missed abortion
MYOM2
SDHA
TPPP
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844023060760

Similar Items

Similar Items