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

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Showing items 1-10 of 15 (2 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2020-12-16T02:26:26Z	Human α-L-iduronidase (IDUA) gene: Apparent recombination in intron 2 by haplotype analysis in a Taiwanese population	Lee-Chen G.-J.; Wang T.-R.; WUH-LIANG HWU; Day K.-R.; Wang C.-K.
臺大學術典藏	2020-12-16T02:26:22Z	Identification and characterization of -3c-g acceptor splice site mutation in human α-L-iduronidase associated with mucopolysaccharidosis type IH/S	Teng Y.N.;Wang T.R.;Wuh-Liang Hwu;Lin S.P.;Lee-Chen G.J.; Teng Y.N.; Wang T.R.; WUH-LIANG HWU; Lin S.P.; Lee-Chen G.J.
臺大學術典藏	2020-12-16T02:26:10Z	DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients	Wang C.K.;Wu Y.R.;Wuh-Liang Hwu;Chen C.M.;Ro L.S.;Chen S.T.;Gwinn-Hardy K.;Yang C.C.;Wu R.M.;Chen T.F.;Wang H.C.;Chao M.C.;Chiu M.J.;Lu C.J.;Lee-Chen G.J.; Wang C.K.; Wu Y.R.; WUH-LIANG HWU; Chen C.M.; Ro L.S.; Chen S.T.; Gwinn-Hardy K.; Yang C.C.; Wu R.M.; Chen T.F.; Wang H.C.; Chao M.C.; Chiu M.J.; Lu C.J.; Lee-Chen G.J.
臺大學術典藏	2020-03-04T05:35:18Z	DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients	Wang C.K.; Wu Y.R.; Hwu W.L.; Chen C.M.; Ro L.S.; Chen S.T.; Gwinn-Hardy K.; Yang C.C.; Wu R.M.; Chen T.F.; Wang H.C.; Chao M.C.; MING-JANG CHIU; Lu C.J.; Lee-Chen G.J.
臺大學術典藏	2020-03-03T01:14:51Z	DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients	Wang C.K; Wu Y.R; Hwu W.L; Chen C.M; Ro L.S; Chen S.T; Gwinn-Hardy K; Yang C.C; Wu R.M; TA-FU CHEN; Wang H.C; Chao M.C; Chiu M.J; Lu C.J; Lee-Chen G.J.
臺大學術典藏	2020-02-25T08:01:45Z	DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients	Wang C.K;Wu Y.R;Hwu W.L;Chen C.M;Ro L.S;Chen S.T;Gwinn-Hardy K;Yang C.C;Ruey-Meei Wu;Chen T.F;Wang H.C;Chao M.C;Chiu M.J;Lu C.J;Lee-Chen G.J.; Wang C.K; Wu Y.R; Hwu W.L; Chen C.M; Ro L.S; Chen S.T; Gwinn-Hardy K; Yang C.C; RUEY-MEEI WU; Chen T.F; Wang H.C; Chao M.C; Chiu M.J; Lu C.J; Lee-Chen G.J.
臺大學術典藏	2020-02-25T08:01:45Z	DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients	Wang C.K;Wu Y.R;Hwu W.L;Chen C.M;Ro L.S;Chen S.T;Gwinn-Hardy K;Yang C.C;Ruey-Meei Wu;Chen T.F;Wang H.C;Chao M.C;Chiu M.J;Lu C.J;Lee-Chen G.J.; Wang C.K; Wu Y.R; Hwu W.L; Chen C.M; Ro L.S; Chen S.T; Gwinn-Hardy K; Yang C.C; RUEY-MEEI WU; Chen T.F; Wang H.C; Chao M.C; Chiu M.J; Lu C.J; Lee-Chen G.J.
臺大學術典藏	2020-02-25T08:01:43Z	The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairment	Lin I.-S;Ruey-Meei Wu;Lee-Chen G.-J;Shan D.-E;Gwinn-Hardy K.; Lin I.-S; RUEY-MEEI WU; Lee-Chen G.-J; Shan D.-E; Gwinn-Hardy K.
臺大學術典藏	2020-02-25T08:01:43Z	The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairment	Lin I.-S;Ruey-Meei Wu;Lee-Chen G.-J;Shan D.-E;Gwinn-Hardy K.; Lin I.-S; RUEY-MEEI WU; Lee-Chen G.-J; Shan D.-E; Gwinn-Hardy K.
臺大學術典藏	2020-02-25T08:01:42Z	Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease	Ross O.A;Wu Y.-R;Lee M.-C;Funayama M;Chen M.-L;Soto A.I;Mata I.F;Lee-Chen G.-J;Chiung M.C;Tang M;Zhao Y;Hattori N;Farrer M.J;Tan E.-K;Ruey-Meei Wu; Ross O.A; Wu Y.-R; Lee M.-C; Funayama M; Chen M.-L; Soto A.I; Mata I.F; Lee-Chen G.-J; Chiung M.C; Tang M; Zhao Y; Hattori N; Farrer M.J; Tan E.-K; RUEY-MEEI WU

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