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Advancing precision care in pregnancy through an actionable fetal findings list

2024-09-30

Abstract excerpt

<h4>Summary</h4> The use of genomic sequencing (GS) for prenatal diagnosis of fetuses with sonographic abnormalities has grown tremendously over the past decade. Fetal GS also offers an opportunity to identify incidental genomic variants that are unrelated to the fetal phenotype, but may be relevant to fetal and newborn health. There are currently no guidelines for reporting incidental findings from fetal GS. In t...

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Identifiers and source

Literature Corpus work
fb49424b-9b15-5e02-b0f5-8c662f9cfa8c
DOI
10.1101/2024.09.26.24314442
Open publication

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Advancing precision care in pregnancy through an actionable fetal findings listDOI 10.1101/2024.09.26.24314442
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