P477: An amplification-based, nanopore carrier screening panel resolves clinically-relevant variants in CFTR, SMN1/2, HBA1/2, HBB, and FMR1 in a unified workflow
Shranjeno v:
| Principais autores: | , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Elsevier
2023-01-01
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| Serija: | Genetics in Medicine Open |
| Online dostop: | http://www.sciencedirect.com/science/article/pii/S2949774423005241 |
| Oznake: |
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