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"wang 陳持平；chih ping chen；shuan "
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| 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
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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
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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
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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 |
Showing items 1-3 of 3 (1 Page(s) Totally)
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