|
English
|
正體中文
|
简体中文
|
总笔数 :0
|
|
造访人次 :
53138497
在线人数 :
630
教育部委托研究计画 计画执行:国立台湾大学图书馆
|
|
|
"wang b b t"的相关文件
显示项目 1-4 / 4 (共1页)
1
每页显示[10|25|50]项目
| 臺大學術典藏 |
2018-09-10T07:02:24Z |
A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: Possible correlation with poor response to fetal therapy
|
Ma, G.-C.;Liu, C.-S.;Chang, S.-P.;Yeh, K.-T.;Ke, Y.-Y.;Chen, T.-H.;Wang, B.B.-T.;Kuo, S.-J.;Shih, J.-C.;Chen, M.; MING CHEN; JIN-CHUNG SHIH |
| 臺大學術典藏 |
2018-09-10T06:41:40Z |
Comparison of immunohistochemical and fluorescence in situ hybridization assessment for HER-2/neu status in Taiwanese breast cancer patients
|
Kuo, S.-J.;Wang, B.B.-T.;Chang, C.-S.;Chen, T.-H.;Yeh, K.-T.;Lee, D.-J.;Yin, P.-L.;Chen, M.; MING CHEN |
| 臺大學術典藏 |
2018-09-10T06:06:47Z |
Prenatal identification of small supernumerary marker chromosomes by FISH in an infant born with mild congenital anomalies [8]
|
Chen, M.;Chang, S.-P.;Yin, P.-L.;Sapeta, M.;Barringer, S.;Kuo, S.-J.;Yu, H.-T.;Wang, B.B.-T.; MING CHEN |
| 臺大學術典藏 |
2018-09-10T05:03:07Z |
Prenatal diagnosis of a fetus affected with down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping
|
Hsieh, L.-J.;Hsieh, T.-C.;Yeh, G.-P.;Lin, M.-I.;Chen, M.;Wang, B.B.-T.; MING CHEN |
显示项目 1-4 / 4 (共1页)
1
每页显示[10|25|50]项目
|
