P293: Long read sequencing analysis of 120 samples with known and challenging-to-detect clinical variants
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| Principais autores: | , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Elsevier
2024-01-01
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| Serier: | Genetics in Medicine Open |
| Online adgang: | http://www.sciencedirect.com/science/article/pii/S2949774424003352 |
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