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Showing items 31-33 of 33 (1 Page(s) Totally)
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| 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
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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.
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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
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Tsai, FJ; Hwu, WL; Lin, SP; Chang, JG; Wang, TR; Tsai, CH |
Showing items 31-33 of 33 (1 Page(s) Totally)
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