English  |  正體中文  |  简体中文  |  0  
???header.visitor??? :  50935827    ???header.onlineuser??? :  975
???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???

"tsai fj"???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 291-315 of 327  (14 Page(s) Totally)
<< < 5 6 7 8 9 10 11 12 13 14 > >>
View [10|25|50] records per page

Institution Date Title Author
中國醫藥大學 2000 Molecular analysis of the N-acetylgalactosamina-6-sulfate sulfatase gene in Taiwanese patients with Mucopolysaccharidosis IVA. Yang, CF; Tsai, FJ; Lin, SP; Wu, JY
中國醫藥大學 2000 Cytogenetic study of workers exposed to chromium compounds Wu, FY; Tsai, FJ; Kuo, HW; Tsai, CH; Wu, WY; Wang, RY; Lai, JS
中國醫藥大學 2000 Distributions of p53 codon 72 polymorphism in bladder cancer - proline form is prominent in invasive tumor Chen, WC; Tsai, FJ; Wu, JY; Wu, HC; Lu, HF; Li, CW
中國醫藥大學 2000 A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia Tsai, FJ; Wu, JY; Lin, WD; Tsai, CH
中國醫藥大學 2000 Infantile form G(M1) gangliosidosis with dilated cardiomyopathy: a case report Lin, HC; Tsai, FJ; Shen, WC; Tsai, CH; Peng, CT
中國醫藥大學 2000 A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) causes non-syndromic craniosynostosis Tsai, FJ; Wu, JY; Lee, CC; Tsai, CH
中國醫藥大學 2000 Antley-Bixler syndrome associated with Arnold-Chiari malformation Chang, YT; Tsai, FJ; Shen, WC; Lin, HC; Peng, CT; Tsai, CH
中國醫藥大學 2000 Breech deformation complex in neonates Hsieh, YY; Tsai, FJ; Lin, CC; Chang, FCC; Tsai, CH
中國醫藥大學 2000 Breech deformation complex in neonates Hsieh, YY; Tsai, FJ; Lin, CC; Chang, FCC; Tsai, CH
中國醫藥大學 2000 Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency Lee, HH; Chang, JG; Tsai, CH; Tsai, FJ; Chao, HT; Chung, BC
中國醫藥大學 2000 Mutation analysis of thyroid peroxidase gene in Taiwanese patients with total iodide organification defects: Identification of five novel mutations. Wu, J; Yang, CF; Tsai, FJ
中國醫藥大學 2000 Aberrant transcripts of FHIT, TSG101 and PTEN/MMAC1 genes in normal peripheral mononuclear cells Wang, NM; Chang, JG; Liu, TC; Lin, SF; Peng, CT; Tsai, FJ; Tsai, CH
中國醫藥大學 2000 Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency Lee, HH; Chang, JG; Tsai, CH; Tsai, FJ; Chao, HT; Chung, BC
中國醫藥大學 1999 Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data Tsai, FJ; Tsai, CH; Chang, JG; Wu, JY
中國醫藥大學 1999 Identification of a common N540K mutation in 8/18 Taiwanese hypochondroplasia patients: further evidence for genetic heterogeneity Tsai, FJ; Wu, JY; Tsai, CH; Chang, JG
中國醫藥大學 1999 Bcl 10 is not commonly mutated in multiple primary solid tumors. Chang, JG; Lee, HH; Wang, NM; Yeh, KT; Tsai, FJ; Tsai, CH
中國醫藥大學 1999 Further characterization of Wilson disease in Taiwan: identification of two novel mutations and high correlation between haplotype and mutation. Wu, JY; Tsai, FJ; Lee, CC; Chang, JG; Tsai, CH
中國醫藥大學 1999 Different race, different face: minor anomalies in Chinese newborn infants Tsai, FJ; Tsai, CH; Peng, CT; Wu, JY; Lien, CH; Wang, TR
中國醫藥大學 1999 Prenatal diagnosis of dyssegmental dysplasia - A case report Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, FJ; Tsai, CH
中國醫藥大學 1999 Molecular analysis of secretor type alpha(1,2)-fucosyltransferase gene mutations in the Chinese and Thai populations Chang, JG; Yang, TY; Liu, TC; Lin, TP; Hu, CJ; Kao, MC; Wang, NM; Tsai, FJ; Peng, CT; Tsai, CH
中國醫藥大學 1999 Molecular analysis of secretor type alpha(1,2)-fucosyltransferase gene mutations in the Chinese and Thai populations Chang, JG; Yang, TY; Liu, TC; Lin, TP; Hu, CJ; Kao, MC; Wang, NM; Tsai, FJ; Peng, CT; Tsai, CH
中國醫藥大學 1999 Prenatal diagnosis of dyssegmental dysplasia - A case report Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, FJ; Tsai, CH
中國醫藥大學 1998 Mutation analysis in fibroblast growth factor receptor genes: Chinese data Lin, SP; Tsai, FJ; Wu, JY; Peng, CT; Tsai, CH
中國醫藥大學 1998 Mutation analysis of Chinese patients with Wilson disease Tsai, FJ; Wu, JY; Chang, JG; Lin, SP; Peng, CT; Tsai, CH
中國醫藥大學 1998 Molecular diagnosis of patients with beta-thalassemia major in central Taiwan by amplified created restriction site analysis Peng, CT; Wu, JY; Tsai, CH; Tsai, FJ; Chang, JG

Showing items 291-315 of 327  (14 Page(s) Totally)
<< < 5 6 7 8 9 10 11 12 13 14 > >>
View [10|25|50] records per page