|
English
|
正體中文
|
简体中文
|
总笔数 :2854334
|
|
造访人次 :
53351253
在线人数 :
438
教育部委托研究计画 计画执行:国立台湾大学图书馆
|
|
|
"wang 陳持平；chih ping chen；shuan "的相关文件
显示项目 1-3 / 3 (共1页)
1
每页显示[10|25|50]项目
| 亞洲大學 |
2017-06 |
Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia
|
Wang, 陳持平；Chih-Ping Chen；Shuan-Pei Li；Shuan-Pei Lin；Yu-Peng Liu；Yu-Peng Liu；Schu-Rern Ch；Schu-Rern Chern；Shin-Wen Che；Shin-Wen Chen；Shih-Ting La；Shih-Ting Lai；Wayseen Wang；Wayseen |
| 亞洲大學 |
2017-02 |
Familial transmission of recurrent 15q11.2 ；BP1-BP2 microdeletion encompassing NIPA1, NIPA2, CYFIP1 and TUBGCP5 associated with phenotypic variability in developmental, speech and motor delay
|
Wang, 陳持平；Chih-Ping Chen；Shuan-Pei Li；Shuan-Pei Lin；Chung-Lin Le；Chung-Lin Lee；Schu-Rern Ch；Schu-Rern Chern；Peih-Shan Wu；Peih-Shan Wu；Yen-Ni Chen；Yen-Ni Chen；Shin-Wen Che；Shin-Wen Chen；Wayseen Wang；Wayseen |
| 亞洲大學 |
2017-02 |
Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6 and BUB1 associated with autism spectrum disorder, intellectual disability and liver disorder
|
Wang, 陳持平；Chih-Ping Chen；Shuan-Pei Li；Shuan-Pei Lin；Chung-Lin Le；Chung-Lin Lee；Schu-Rern Ch；Schu-Rern Chern；Peih-Shan Wu；Peih-Shan Wu；Yen-Ni Chen；Yen-Ni Chen；Shin-Wen Che；Shin-Wen Chen；Wayseen Wang；Wayseen |
显示项目 1-3 / 3 (共1页)
1
每页显示[10|25|50]项目
|
