Whole-exome sequencing applications in prenatal diagnosis of fetal bowel dilatation
This study introduced whole-exome sequencing (WES) in prenatal diagnosis of fetal bowel dilatation to improve the detection outcome when karyotype analysis and copy number variation sequencing (CNV-seq) were uninformative in detecting pathogenic variants. The work reviewed 28 cases diagnosed with fe...
| Published in: | Open Life Sciences |
|---|---|
| Main Authors: | , , , , , , , , |
| Format: | Article |
| Language: | English |
| Published: |
De Gruyter
2023-05-01
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| Subjects: | |
| Online Access: | https://doi.org/10.1515/biol-2022-0598 |
