Clinical utility of trio whole exome sequencing in fetuses with ultrasound anomalies
Abstract Introduction Ultrasound scanning anomalies in fetuses are a cause for concern and often necessitate further diagnostic procedures. This retrospective study evaluated the utility of trio whole exome sequencing (trio-WES) in the diagnosis of fetuses with ultrasound anomalies. Methods We inclu...
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| Autors principals: | , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMC
2025-04-01
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| Col·lecció: | Human Genomics |
| Matèries: | |
| Accés en línia: | https://doi.org/10.1186/s40246-025-00745-6 |
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