Copy number variation characterization and possible candidate genes in miscarriage and stillbirth by next‐generation sequencing analysis

BACKGROUND: The present study aimed to explore the etiological relationship between miscarriage and stillbirth and copy number variations (CNVs), as well as provide useful genetic guidance for high‐risk pregnancy. METHODS: In total, 659 fetal samples were recruited and subjected to DNA extraction an...

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Detalles Bibliográficos
Autores principales: Zhang, Xia, Huang, Qingyan, Yu, Zhikang, Wu, Heming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285438/
https://www.ncbi.nlm.nih.gov/pubmed/34342101
http://dx.doi.org/10.1002/jgm.3383

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285438/
https://www.ncbi.nlm.nih.gov/pubmed/34342101
http://dx.doi.org/10.1002/jgm.3383

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