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Hsiao KJ, Chiang SH. Interlaboratory
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Liu TT, Lu SF, Hsiao KJ. Genonic
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Hsiao KJ, Liu TT, Lu SF, Wu SJ, Wu KF,
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Shiue HS, Chang CL, Chang PL, Wang SS, Lin AP, Wu
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Chen WY, Chen CH, Tsao T, Hsiao KJ.
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Chiang PH, Hsiao KJ, Chuo YT, Liu
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Hsiao KJ, Liu TT, Chang YH, Chiou
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Hsiao KJ, Chiang SH, Wu SJ, Wu KF.
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Wu SJ, Qiu DF, Hsiao KJ.
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Chang YS, Liu TT, Chiang SH, Wu KF, Hsiao KJ.
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Hsiao KJ, Chang YH, Liu TT, Liu MY, Chiang
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Hsiao KJ, Wu SJ, Qiu DF. Prenatal
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Hsiao KJ, Liu TT, Chang YH, Liu MY, Chiang
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Lee SF, Liu TT, Wu SJ, Hsiao KJ.
Mutation analysis of mut gene in Chinese methylmalonic acidemia caused
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2000; P7. |
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Liu MY, Chen CH, Wu SJ, Hsieh YT, Liu TT, Hsiao
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Liu HL, Liu TT, Wu SJ, Toung LC, Qu XB, Hsiao
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Chen CY, Su JS, Chang HM, Chao KM, Hsiao KJ,
Tsai SF. The complete genome sequence of the human ADH gene
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Hsiao KJ, Chen CY, Chang HM, Wu KM, Chiang
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Liu TT, Chang YH, Chiu YH, Chuang SH, Chen CY,
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Tsai SF,Chang HM, Chen CY, Yeh SH, Lin CH, Yang
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Liu TT, Hsiao KJ.
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Chinese Congress of Clinical Chemistry & Laboratory Medicine 2000,
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Okano Y, Asada M, Imamura T, Ohtake A, Murayama K, Choeh K, Hsiao
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Yu WM, Liu TT, Chang M, Zhou ZS, Shen M, Hsiao KJ.
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Chen CH, Tsai MT, Hung CC, Tsai CY, Liu MY, Chen YH, Hsiao
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| 205. |
Qi Y, Liu TT, Chiang SH, Pan H, Zhang Y, Wang CX, Lu JJ, Bao
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| 206. |
Lin CH, Liu MY, Chiang SH, Hsiao KJ. Common
1034>A mutation of galactose-1-phosphate uridyl transferase (GALT)
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2001; P417. |
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Yen PF, Liu MY, Liu TT, Hsiao KJ. The complete
genomic sequence of human DHPR gene and the mutation 697A>C detected
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Conference of Biomedical Sciences, Taipei, 2001; P417. |
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Chiu YH, Liu TT, Liu MY, Hsiao KJ. Molecular
characterization of F40L mutation in Chinese
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Chiang SH, Wu KF, Hsiao KJ. Quality Assurance
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Liu TT, Chiang SH, Wu SJ, Hsiao KJ. Screening
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Liu YN, Liu TT, Wu SJ, Hsiao KJ. Mutation
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Lin CH, Liu TT, Hsiao KJ. Assessment of
electronic data collection from PubMed for the establishment of Chinese
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HGM2002, Shanghai, 2002;320. |
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Liu TT, Yen PF, Lin CH, Chiang SH, Chen CY, Tsai SF, Hsiao
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clone 395N09: The complete genomic sequence of dihydropteridine
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HGM2002, Shanghai, 2002;321. |
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Liu MY, Chen CH, Wu SJ, Hsieh YT, Liu TT, Hsiao KJ.
Identification and characterization of alpha-galactosidase a mutations
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| 215. |
Liu TT, Lin CH, Liu MY, Chern SR, Chiang SH, Hsiao KJ.
Two novel mutations, 1034C>A and IVS9+1G>T, of
galactose-1-phosphate uridyltransferase (GALT) gene identified in
Chinese galactosemia. 8th Annual Asia-European Workshop of Inborn
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Kobayashi K, Okano Y, Nishi I, Lu YB, Choeh K, Hsiao KJ,
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mutated SLC25A13 gene in East Asia. 45th annual meeting of
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Touma EH, Romstad A, Khneisser I, Hsiao KJ, Loiselet
J, Dhondt JL. Epidemiology of hyperphenylalaninemia (HPA) in
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Hsiao KJ, Liu TT. Gene diagnosis
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Teng YT, Wu SJ, Lam WF, Liu TT, Hsiao KJ.
Identification of three methylmalonyl CoA mutase gene mutations
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18th Joint Annual Conference of Biomedical Sciences, Taipei, 2003;P440.
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Hsiao KJ, Lin CH, Fan JW, Tu CH,
Chiang SH, Liu TT. Development of the Chinese Gene Variation
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Liu TT, Chiu YH, Chang YC,
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