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Showing items 291-327 of 327 (7 Page(s) Totally)
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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
中國醫藥大學	1998	Prenatal diagnosis of Apert syndrome	Chang, CC; Tsai, FJ; Tsai, HD; Tsai, CH; Hsieh, YY; Lee, CC; Yang, TC; Wu, JY
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
中國醫藥大學	1998	Molecular analysis of type I oculocutaneous albinism in Chinese	Wu, JY; Lin, SP; Tsai, LP; Tsai, FJ; Peng, CT; Tsai, CH
中國醫藥大學	1998	Rotavirus associated with poliomyelitis-like syndrome	Chou, IC; Tsai, CH; Tsai, FJ
中國醫藥大學	1998	Myelination arrest demonstrated using magnetic resonance imaging in a child with type I G(M1) gangliosidosis	Shen, WC; Tsai, FJ; Tsai, CH
中國醫藥大學	1997	Mutations in fibroblast growth factor receptor genes: Chinese data.	Tsai, FJ; Wu, JY; Peng, CT; Tsai, CH
中國醫藥大學	1996	Catabolic effect in premature infants with early dexamethasone treatment	Tsai, FJ; Tsai, CH; Wu, SF; Liu, YH; Yeh, TF
中國醫藥大學	1996	Detection of congenital cytomegalovirus infection in Chinese newborn infants using polymerase chain reaction	Tsai, CH; Tsai, FJ; Shih, YT; Wu, SF; Liu, SC; Tseng, YH
中國醫藥大學	1996	X-linked recessive myotubular myopathy proven by muscle biopsy	Tsai, CH; Huang, WS; Tsai, FJ; Lee, CC; Chen, SS
中國醫藥大學	1996	X-linked recessive myotubular myopathy proven by muscle biopsy	Tsai, CH; Huang, WS; Tsai, FJ; Lee, CC; Chen, SS
中國醫藥大學	1993	MINOR ANOMALIES IN CHINESE NEWBORN-INFANTS	TSAI, FJ; TSAI, CH
中國醫藥大學	1992	NOMA NEONATORUM - AN UNUSUAL CASE OF NOMA INVOLVING A FULL-TERM NEONATE	LIN, JY; WANG, DW; PENG, CT; TSAI, FJ; CHIOU, YM; TSAI, CH

Showing items 291-327 of 327 (7 Page(s) Totally)
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