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Low-pass genome sequencing reveals associations between copy number variations and fetal ultrasonographic anomalies and soft markers in a cohort of 43,721 fetuses

2022-11-17

Abstract excerpt

<h4>Objective: </h4> To systematically explore the association between pathogenic/likely pathogenic copy number variations (pCNV) and ultrasonographic anomalies and soft markers. Design Retrospective cohort study. Setting Data were obtained from multiple centers in china. Population or Sample Fetuses performed low-pass genome sequencing and ultrasonography between 2016 and 2020. Method The yields of pCNV under var...

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Literature Corpus work
6081fbe7-5856-5e40-b03f-db89e6cbcbff
DOI
10.22541/au.166870119.97359613/v1
Open publication

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Low-pass genome sequencing reveals associations between copy number variations and fetal ultrasonographic anomalies and soft markers in a cohort of 43,721 fetusesDOI 10.22541/au.166870119.97359613/v1
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