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.
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Accepted: March 6, 2023
Received in revised form: March 1, 2023
Received: November 26, 2022
Publication stageIn Press Accepted Manuscript
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