| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
|---|---|---|---|---|---|---|
| 2010 | Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome | Chang, C. F.; Li, L. H.; Wang, C. H.; Tsai, F. J.; Chen, T. C.; Wu, J. Y.; Chen, Y. T.; Tsai, A. C. H. | American J of Medical Genetics Part A 152A(9), 2365-2371 |
