P764: RNA sequencing improves assessment of variants of uncertain significance from fetal genome and exome sequencing*
| Published in: | Genetics in Medicine Open |
|---|---|
| Main Authors: | , , , , , , , , , , , , , , , |
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-01-01
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| Online Access: | http://www.sciencedirect.com/science/article/pii/S2949774424008185 |
