|
"wang t r"的相關文件
顯示項目 96-105 / 143 (共15頁)
<< < 5 6 7 8 9 10 11 12 13 14 > >>
每頁顯示[10|25|50]項目
| 臺大學術典藏 |
2020-02-03T08:15:30Z |
Maternal and fetal outcome of pregnant women with idiopathic thrombocytopenic purpura: retrospective analysis of 25 pregnancies.
|
Hsiao-Lin Hwa;Chen R.J.;Chen Y.C.;Wang T.R.;Huang S.C.;Chow S.N.; HSIAO-LIN HWA; Chen R.J.; Chen Y.C.; Wang T.R.; Huang S.C.; Chow S.N. |
| 臺大學術典藏 |
2020-02-03T08:15:25Z |
Erratum: Molecular genetic study of Pompe disease in Chinese patients in Taiwan (Human Mutation (1999) 13 (380-384))
|
Ko T.-M.;Hwu W.-L.;Lin Y.-W.;Tseng L.-H.;Hsiao-Lin Hwa;Wang T.-R.;Chuang S.- M.;Hayashi K.; Ko T.-M.; Hwu W.-L.; Lin Y.-W.; Tseng L.-H.; HSIAO-LIN HWA; Wang T.-R.; Chuang S.- M.; Hayashi K. |
| 臺大學術典藏 |
2020-02-03T08:15:24Z |
Molecular genetic study of Pompe disease in Chinese patients in Taiwan
|
Ko T.-M.; Hwu W.-L.; Lin Y.-W.; Tseng L.-H.; HSIAO-LIN HWA; Wang T.-R.; Chuang S.-M.; Ko T.-M.;Hwu W.-L.;Lin Y.-W.;Tseng L.-H.;Hsiao-Lin Hwa;Wang T.-R.;Chuang S.-M. |
| 臺大學術典藏 |
2018-09-10T07:33:03Z |
Corneal opacity and congenital glaucoma associated with massive heparan sulfaturia: Report of one case
|
Lin, S.-C.;Hu, F.-R.;Hou, J.-W.;Yao, Y.-T.;Wang, T.-R.;Hung, P.-T.; FUNG-RONG HU |
| 臺大學術典藏 |
2018-09-10T07:24:56Z |
Molecular genetic study of Pompe disease in Chinese patients in Taiwan
|
Ko, T.-M.;Hwu, W.-L.;Lin, Y.-W.;Tseng, L.-H.;Hwa, H.-L.;Wang, T.-R.;Chuang, S.-M.; LI-HUI TSENG; HSIAO-LIN HWA |
| 臺大學術典藏 |
2018-09-10T07:24:56Z |
Erratum: Molecular genetic study of Pompe disease in Chinese patients in Taiwan (Human Mutation (1999) 13 (380-384))
|
Ko, T.-M.;Hwu, W.-L.;Lin, Y.-W.;Tseng, L.-H.;Hwa, H.-L.;Wang, T.-R.;Chuang S.-, M.;Hayashi, K.; LI-HUI TSENG; HSIAO-LIN HWA |
| 臺大學術典藏 |
2018-09-10T07:22:20Z |
Detection of KAL-1 gene deletion with fluorescence in situ hybridization
|
Hou, J.-W.;Tsai, W.-Y.;Wang, T.-R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T06:14:53Z |
CATCH 22: Deletion of locus 22Q11 in velocardiofacial syndrome, digeorge anomaly, and nonsyndromic conotruncal defects
|
Hou, J.-W.;Wang, J.-K.;Tsai, W.-Y.;Chou, C.-C.;Wang, T.-R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T06:14:53Z |
Partial DiGeorge anomaly associated with 10p deletion
|
Hsu, H.-L.;Hsiao, P.-H.;Hou, J.-W.;Tsai, W.-Y.;Wang, T.-R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T06:06:32Z |
Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutation.
|
Tsai, L.P.;Sue, W.C.;Hwu, W.L.;Lin, K.H.;Wang, T.R.; KAI-HSIN LIN |
顯示項目 96-105 / 143 (共15頁)
<< < 5 6 7 8 9 10 11 12 13 14 > >>
每頁顯示[10|25|50]項目
|
