Whole-Exome Sequencing Reveals Pediatric Rare Syndromic Hearing Loss
Objective To discuss the significance of genetic diagnosis of children with syndromic hearing loss by using whole-exome sequencing. Methods The clinical data of 34 children with sensorineural hearing loss were collected and the whole exons of genome of the children and their parents were sequenced a...
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| Auteurs principaux: | , , , , , |
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| Format: | Artigo |
| Langue: | Chinês |
| Publié: |
Editorial Office of Journal of Rare Diseases
2022-07-01
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| Collection: | 罕见病研究 |
| Sujets: | |
| Accès en ligne: | https://jrd.chard.org.cn/article/doi/10.12376/j.issn.2097-0501.2022.03.008 |
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