Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia
- Type: Whole Genome Sequencing
- Archiver: European Genome-Phenome Archive (EGA)
| Publications | Citations |
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Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia.
J Med Genet 61: 2024 250-261 |
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