| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
|---|---|---|---|---|---|---|
| 2008 | Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia | Lee, M. T.; Tsai, A. C.; Chou, C. H.; Sun, F. M.; Huang, L. C.; Yen, P.; Lin, C. C.; Liu, C. Y.; Wu, J. Y.; Chen, Y. T.; Tsai, F. J. | Genomic Med 2(1-2), 45-49 |
