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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...
Gorde:
| Egile Nagusiak: | , , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Wiley
2019-06-01
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| Saila: | Molecular Genetics & Genomic Medicine |
| Gaiak: | |
| Sarrera elektronikoa: | https://doi.org/10.1002/mgg3.684 |
| Etiketak: |
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