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Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees
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| Publicat a: | Clin Genet |
|---|---|
| Autors principals: | , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6499369/ https://ncbi.nlm.nih.gov/pubmed/30828794 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.13515 |
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