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...

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Detalles Bibliográficos
Autores principales: Zeng, Wen, Qi, Hong, Du, Yang, Cai, Lirong, Wen, Xiaohui, Wan, Qian, Luo, Yao, Zhu, Jianjiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10428042/
https://www.ncbi.nlm.nih.gov/pubmed/37593615
http://dx.doi.org/10.1016/j.heliyon.2023.e18868

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10428042/
https://www.ncbi.nlm.nih.gov/pubmed/37593615
http://dx.doi.org/10.1016/j.heliyon.2023.e18868

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