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"It's probably nothing, but…" Couples' experiences of pregnancy following an uncertain prenatal genetic result

19 Jan 2020

Abstract excerpt

INTRODUCTION: A common concern regarding the introduction of chromosomal microarray in prenatal testing is the concomitant identification of an uncertain copy number variant (CNV) where significance and clinical implication for the unborn child can be difficult or impossible to predict. Following the identification of an uncertain CNV, prospective parents may decide to continue the pregnancy. The aim of this...

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PMID: 31955407
DOI: 10.1111/aogs.13813

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