Article

Noninvasive Prenatal Screening for 22q11.2 Deletion/Duplication Syndrome Using multiplex dPCR

2023-03-27

Abstract excerpt

<title>Abstract</title> <p>Background 22q11.2 deletion/duplication syndrome has a high incidence in prenatal fetuses and cause variety of severe abnormalities. At present, screening for 22q11.2 deletion/duplication syndrome in fetuses is difficult because of the lack of effective targeted programs. Methods In this study, six detection sites and their corresponding probes were designed in the 22q11.2 recurrent r...

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Literature Corpus work: 918d5925-2a12-539f-84b0-f2dd694dbde7
DOI: 10.21203/rs.3.rs-2713860/v1

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