臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Institution	Date	Title	Author
臺大學術典藏	2021-08-23T01:36:01Z	High frequency of two mutations in codon 778 in exon 8 of the ATP7B gene in Taiwanese families with Wilson disease	Chuang L.-M.; HUEY-PEIR WU; Jang M.-H.; Wang T.-R.; Sue W.-C.; Lin B.J.; Cox D.W.; Tai T.-Y.
臺大學術典藏	2020-12-18T02:21:57Z	Electroclinical characteristics of seizures - Comparing Prader-Willi syndrome with Angelman syndrome	Wang P.-J.;Hou J.-W.;Sue W.-C.;Wang-Tso Lee; Wang P.-J.; Hou J.-W.; Sue W.-C.; WANG-TSO LEE
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
國立成功大學	2007-10	Investigation of the stress singularity of a magnetoelectroelastic bonded antiplane wedge	Sue, W. C.; Liou, J. Y.; Sung, Jen-Chun
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.

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