A Boy with Holt-Oram Syndrome Caused by Novel Mutation c.1304delT in the TBX5 Gene.
| Autor: | Muru, K., Kalev, I., Teek, R., Sõnajalg, M., Kuuse, K., Reimand, T., Õunap, K. |
|---|---|
| Zdroj: | Molecular Syndromology; 2010, Vol. 1 Issue 6, p307-310, 4p |
| Databáze: | Complementary Index |
| Externí odkaz: |
|