thymidine has been researched along with BOF Syndrome in 1 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "This is the first report of BOR syndrome caused by deletion mutation of the EYA1 gene in Korea." | 1.35 | A novel frameshift mutation in the EYA1 gene in a Korean family with branchio-oto-renal syndrome. ( Choi, SY; Kim, SC; Kim, UK; Koh, YW; Lee, HJ; Lee, JD, 2009) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lee, JD | 1 |
| Kim, SC | 1 |
| Koh, YW | 1 |
| Lee, HJ | 1 |
| Choi, SY | 1 |
| Kim, UK | 1 |
1 other study available for thymidine and BOF Syndrome
| Article | Year |
|---|---|
A novel frameshift mutation in the EYA1 gene in a Korean family with branchio-oto-renal syndrome.
Topics: Adult; Branchial Region; Branchio-Oto-Renal Syndrome; Ear; Fistula; Frameshift Mutation; Hearing Los | 2009 |