| 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 |
| 臺大學術典藏 |
2018-09-10T05:46:39Z |
Kleine-Levin syndrome in a boy with Prader-Willi syndrome
|
Gau, S.-F.;Soong, W.-T.;Liu, H.-M.;Hou, J.-W.;Tsai, W.-Y.;Chiu, Y.-N.;Yeh, Y.-C.;Wang, P.-J.;Wang, T.-R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T05:46:28Z |
Camptomelic dysplasia: report of one case.
|
Tsao, P.N.;Teng, R.J.;Hwu, W.L.;Tsou Yau, K.I.;Wang, T.R.; PO-NIEN TSAO |
| 臺大學術典藏 |
2018-09-10T05:12:25Z |
Prevalence of permanent primary congenital hypothyroidism in Taiwan.
|
Tsai, W.Y.;Lee, J.S.;Chao, M.C.;Chen, L.Y.;Lin, S.J.;Wu, K.H.;Wang, T.R.;Chen, J.S.;Chuang, S.M.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T04:43:31Z |
Congenital nephrotic syndrome with microcephaly: report of a case.
|
Yu, C.H.;Tsai, W.S.;Wang, P.J.;Tsau, Y.K.;Tseng, G.C.;Wang, T.R.; YONG-KWEI TSAU |
| 臺大學術典藏 |
2018-09-10T04:17:49Z |
DNA fingerprinting in the Chinese with an oligonucleotide probe (GTG)5.
|
Hwu, W.L.;Chen, R.L.;Lin, K.H.;Wang, T.R.; KAI-HSIN LIN |
| 臺大學術典藏 |
2018-09-10T04:05:38Z |
Familial nephrogenic diabetes insipidus: report of two families.
|
Lee, J.S.;Tsai, W.Y.;Tsai, W.S.;Tsau, Y.K.;Chen, C.H.;Wang, T.R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T04:05:21Z |
Familial nephrogenic diabetes insipidus: report of two families.
|
Lee, J.S.;Tsai, W.Y.;Tsai, W.S.;Tsau, Y.K.;Chen, C.H.;Wang, T.R.; YONG-KWEI TSAU |
| 臺大學術典藏 |
2018-09-10T03:41:51Z |
Prader-Willi syndrome with chromosome 15 interstitial deletion: report of one case.
|
Hwu, W.L.;Tsai, W.Y.;Lee, J.S.;Wang, P.J.;Wang, T.R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T03:32:25Z |
Wilson disease presenting as fulminant hepatic failure, acute hemolytic anemia and renal failure: report of one case
|
Tseng, C.L.;Tsai, S.L.;Lin, K.H.;Chang, M.H.;Wang, T.R.;Hsu, Y.H.;Hsu, H.C.; KAI-HSIN LIN |
| 臺大學術典藏 |
2018-09-10T03:24:11Z |
Wiedemann-Beckwith syndrome with congenital central hypothyroidism in one of monozygotic twins.
|
Chien, C.H.;Lee, J.S.;Tsai, W.Y.;Wang, T.R.; WEN-YU TSAI |
| 臺大學術典藏 |
1999 |
Molecular genetic study of Pompe disease in Chinese patients in Taiwan
|
Ko T.-M.;Wuh-Liang Hwu;Lin Y.-W.;Tseng L.-H.;Hwa H.-L.;Wang T.-R.;Chuang S.-M.; Ko T.-M.; WUH-LIANG HWU; Lin Y.-W.; Tseng L.-H.; Hwa H.-L.; Wang T.-R.; Chuang S.-M. |
| 國立成功大學 |
1998-06 |
A curvature-ovalization measurement apparatus for circular tubes under cyclic bending
|
Pan, Wen-Fung; Wang, T. R.; Hsu, C. M. |
| 臺大學術典藏 |
1998 |
Recommendations for management of severe enterovirus infection in Taiwan
|
PING-ING LEE; Lee C.-Y.; Wang T.-R. |
| 臺大學術典藏 |
1996 |
Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutation.
|
Tsai L.P.;Sue W.C.;Wuh-Liang Hwu;Lin K.H.;Wang T.R.; Tsai L.P.; Sue W.C.; WUH-LIANG HWU; Lin K.H.; Wang T.R. |
| 臺大學術典藏 |
1996 |
Hepatoblastoma in an infant with Beckwith-Wiedemann Syndrome.
|
Wang T.R.; Chang M.H.; YEN-HSUAN NI; Hwu W.L.; Jeng Y.M.; Tsai S.Y.;Jeng Y.M.;Hwu W.L.;Yen-Hsuan Ni;Chang M.H.;Wang T.R.; Tsai S.Y. |
