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16p13.11 deletion/duplication: prenatal diagnosis, postnatal outcome follow-up and phenotypic manifestations: a large cohort study

2025-06-06

Abstract excerpt

Abstract <h4>Objective: </h4> To understand phenotyping and prognosis for fetuses with 16p13.11 deletion/duplication in East Asian population. <h4>Design: </h4> Retrospective prenatal and patient cohort study in southern China. <h4>Setting: </h4> Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region. Population: All fetuses and patients underwent chromosomal microarray analysis between April 20...

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Literature Corpus work
f852a790-8eee-572f-981c-f40372a58634
DOI
10.22541/au.174919691.11919534/v1
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