Analysis of copy number variants detected by sequencing in spontaneous abortion
Analysis of copy number variants detected by sequencing in spontaneous abortion
About this item
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Author / Creator
Liu, Anhui , Zhou, Liyuan , Huang, Yazhou and Peng, Dan
Publisher
England: BioMed Central Ltd
Journal title
Language
English
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Publisher
England: BioMed Central Ltd
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Contents
The incidence of spontaneous abortion (SA), which affects approximately 15-20% of pregnancies, is the most common complication of early pregnancy. Pathogenic copy number variations (CNVs) are recognized as potential genetic causes of SA. However, CNVs of variants of uncertain significance (VOUS) have been identified in products of conceptions (POCs...
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Full title
Analysis of copy number variants detected by sequencing in spontaneous abortion
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TN_cdi_doaj_primary_oai_doaj_org_article_eb43b69c8ea349bca659aea0c48fefb1
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_eb43b69c8ea349bca659aea0c48fefb1
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ISSN
1755-8166
E-ISSN
1755-8166
DOI
10.1186/s13039-024-00683-3