Unstructured abstract
Fetal malformations have a variable prognosis which may be influenced by the detection
of an underlying monogenic etiology. The careful detection and selection of fetal
phenotypes and the use of prenatal Next Generation Sequencing with robust bioinformatic
pathways and variant selection improve clinical utility and impact.
Keywords
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Article info
Publication history
Accepted:
March 6,
2023
Received in revised form:
March 1,
2023
Received:
November 26,
2022
Publication stage
In Press Accepted ManuscriptIdentification
Copyright
Crown Copyright © 2023 Published by Elsevier Inc. All rights reserved.
