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Showing items 26-33 of 33  (2 Page(s) Totally)
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Institution Date Title Author
國立臺灣大學 2005-04 Six novel NPC1 mutations in Chinese patients with Niemann–Pick disease type C Yang, CC; Su, YN; Chiou, PC; Fietz, MJ; Yu, CL; Hwu, WL; Lee, MJ
國立臺灣大學 2005-02 Mapping of psoriasis to 17q terminus Hwu, WL; Yang, CF; Fann, CS; Chen, CL; 蔡呈芳; Chien, YH; Chiang, SC; Chen, CH; Hung, SI; Wu, JY; Chen, YT
國立臺灣大學 2004-07 DNA haplotype analysis of CAG repeat in Taiwanese Huntington’s disease patients Wang, CK; Wu, YR; Hwu, WL; Chen, CM; Ro, LS; Chen, ST; Gwinn-Hardy, K; Yang, CC; Wu, RM; Chen, TF; Wang, HC; Chao, MC; Chiu, MJ; Lu, CJ; Lee-Chen, GJ
臺北醫學大學 2004 DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients 汪漢澄; Wang CK; Wu YR; Hwu WL; Chen CM; Ro LS; Chen ST. Gwinn-Hardy K. Yang CC. Wu RM. Chen TF. Wang HC. Chao MC. Chiu MJ. Lu CJ. Lee-Chen GJ
臺北醫學大學 2004 DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients 汪漢澄; Wang CK; Wu YR; Hwu WL; Chen CM; Ro LS; Chen ST. Gwinn-Hardy K. Yang CC. Wu RM. Chen TF. Wang HC. Chao MC. Chiu MJ. Lu CJ. Lee-Chen GJ
中國醫藥大學 2004 Detection of a homozygous D645E mutation of the acid alpha-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II Chen, CP; Lin, SP; Tzen, CY; Tsai, FJ; Hwu, WL; Wan, WS
國立臺灣大學 2000-07 Metabolic disorders mimicking Reye syndrome. Chang, PF; Huang, SF; Hwu, WL; Hou, JW; Ni, YH; Chang, MH.
中國醫藥大學 1998 Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with apert syndrome Tsai, FJ; Hwu, WL; Lin, SP; Chang, JG; Wang, TR; Tsai, CH

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