| No | 記事 | 記事著者 |
|---|
| 1 | Mutations in a Novel Gene with Transmembrane Domains Underlie Usher Syndrome Type 3 | Tarja Joensuu, Riikka Hamakainen, ... |
| 2 | Novel TFAP2B Mutations That Cause Char Syndrome Provide a Genotype-Phenotype Correlation | Feng Zhao, Constance G. Weismann, ... |
| 3 | Germline Mutations in BMPR1A/ALK3 Cause a Subset of Causes of Juvenile Polyposis Syndrome and of Cowden and ... | Xiao-Ping Zhou, Kelly Woodford-Richens, ... |
