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Clinical utility in infants with suspected monogenic conditions through next‐generation sequencing
Abstract Background Rare diseases are complex disorders with huge variability in clinical manifestations. Decreasing cost of next‐generation sequencing (NGS) tests in recent years made it affordable. We witnessed the diagnostic yield and clinical use of different NGS strategies on a myriad of monoge...
Na minha lista:
| Main Authors: | , , , , , , , |
|---|---|
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Wiley
2019-06-01
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| Sraith: | Molecular Genetics & Genomic Medicine |
| Ábhair: | |
| Rochtain Ar Líne: | https://doi.org/10.1002/mgg3.684 |
| Clibeanna: |
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