English  |  正體中文  |  简体中文  |  2809389  
???header.visitor??? :  26997586    ???header.onlineuser??? :  471
???header.sponsordeclaration???
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
???ui.leftmenu.abouttair???

???ui.leftmenu.bartitle???

???index.news???

???ui.leftmenu.copyrighttitle???

???ui.leftmenu.link???

"bali d s"???jsp.browse.items-by-author.description???

???jsp.browse.items-by-author.back???
???jsp.browse.items-by-author.order1??? ???jsp.browse.items-by-author.order2???

Showing items 1-7 of 7  (1 Page(s) Totally)
1 
View [10|25|50] records per page

Institution Date Title Author
臺大學術典藏 2021-01-21T02:05:00Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; CHIEN-YI CHEN; Hsieh W.-S.; Tsao P.-N.; Chen Y.-T.; Lee N.-C.
臺大學術典藏 2020-12-24T06:16:51Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Lee N.-C.; Chen Y.-T.; Tsao P.-N.; Hsieh W.-S.; Chen C.-Y.; Chou H.-C.; Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; YIN-HSIU CHIEN
臺大學術典藏 2020-12-24T02:03:54Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Lee N.-C.; Chen Y.-T.; Tsao P.-N.; Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; HUNG-CHIEH CHOU; Chen C.-Y.; Hsieh W.-S.
臺大學術典藏 2020-12-22T03:29:29Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Lee N.-C.; Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; Chen C.-Y.; Hsieh W.-S.; PO-NIEN TSAO; Chen Y.-T.
臺大學術典藏 2020-12-16T02:25:38Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Li S.-C.; WUH-LIANG HWU; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; Chen C.-Y.; Hsieh W.-S.; Tsao P.-N.; Chen Y.-T.; Lee N.-C.
臺大學術典藏 2020-12-09T01:38:32Z Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; Chen C.-Y.; Hsieh W.-S.; Tsao P.-N.; Chen Y.-T.; NI-CHUNG LEE
實踐大學 2009 Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder Li, S.C.;Chen, C.M.;Goldstein, J.L.;Wu, J.Y.;Lemyre, E.;Burrow, T.A.;Kang, P.B.;Chen, Y.T.;Bali, D.S.

Showing items 1-7 of 7  (1 Page(s) Totally)
1 
View [10|25|50] records per page