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機構	日期	題名	作者
中國醫藥大學	2003	Growth hormone (GH) deficiency in patients with beta-thalassemia major and the efficacy of recombinant GH treatment	Wu, KH; Tsai, FJ; Peng, CT
中國醫藥大學	2003	The lack of association between febrile convulsions and polymorphisms in SCN1A	Chou, IC; Peng, CT; Tsai, FJ; Huang, CC; Shi, YR; Tsai, CH
中國醫藥大學	2003	Association of interleukin 10 and receptor antagonist gene polymorphisms with primary open-angle glaucoma	Lin, HJ; Tsai, SC; Tsai, FJ; Chen, WC; Tsai, JJP; Hsu, CD
中國醫藥大學	2003	TAP1 gene Accl polymorphism is associated with atopic bronchial asthma	Hang, LW; Hsia, TC; Chen, WC; Chen, HY; Tsai, FJ
中國醫藥大學	2003	Androgen receptor (AR) gene microsatellite polymorphism in postmenopausal women: correlation to bone mineral density and susceptibility to osteoporosis	Chen, HY; Chen, WC; Wu, MC; Tsai, FJ; Tsai, CH
中國醫藥大學	2003	Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency	Lee, HH; Chang, SF; Tsai, FJ; Tsai, LP; Lin, CY
中國醫藥大學	2003	Insulin-like growth factor-II gene polymorphism is associated with primary open angle glaucoma	Tsai, FJ; Lin, HJ; Chen, WC; Chen, HY; Fan, SS
中國醫藥大學	2002	Characterization of four novel b-galactosidase gene mutations and a polymorphism in Taiwanese patients with GMI-gangliosidosis.	Wu, JY; Yang, CF; Tsai, FJ
中國醫藥大學	2002	Association between angiotensinogen gene M235T polymorphism and mitral valve prolapse syndrome in Taiwan Chinese	Chou, HT; Hung, JS; Chen, YT; Shi, YR; Tsai, FJ
中國醫藥大學	2002	Lack of association between transforming growth factor-beta 1 gene polymorphisms and mitral valve prolapse in Taiwan Chinese	Chou, HT; Shi, YR; Hsu, Y; Tsai, FJ
中國醫藥大學	2002	Correlation of p21 gene codon 31 polymorphism and TNF-alpha gene polymorphism with nasopharyngeal carcinoma	Tsai, MH; Chen, WC; Tsai, FJ
中國醫藥大學	2002	Cytochrome P450c17 alpha (CYP17) gene polymorphism is not associated with leiomyoma susceptibility	Hsieh, YY; Tsai, FJ; Chang, CC; Tsai, CH; Lin, CC; Yeh, LS
中國醫藥大學	2002	The polymorphisms of codon 727 and 52 of thyroid-stimulating hormone receptor gene are not associated with mitral valve prolapse syndrome in Taiwan Chinese	Chou, HT; Shi, YR; Chang, CT; Tsai, FJ
中國醫藥大學	2002	Smith-Magenis syndrome with bilateral vesicoureteral reflux: A case report	Chou, IC; Tsai, FJ; Yu, MT; Tsai, CH
中國醫藥大學	2002	Interleukin-4 intron 3 polymorphism is not related to susceptibility to febrile seizures	Tsai, FJ; Chou, IC; Hsieh, YY; Lee, CC; Lin, CC; Tsai, CH
中國醫藥大學	2002	Polymorphisms for interleukin 1 beta exon 5 and interleukin 1 receptor antagonist in Taiwanese children with febrile convulsions	Tsai, FJ; Hsieh, YY; Chang, CC; Lin, CC; Tsai, CH
中國醫藥大學	2002	Polymorphisms for interleukin-4 (IL-4)-590 promoter, IL-4 intron3, and tumor necrosis factor alpha-308 promoter: Non-association with endometriosis	Hsieh, YY; Chang, CC; Tsai, FJ; Hsu, Y; Tsai, HD; Tsai, CH
中國醫藥大學	2002	Angiotensin h type 1 receptor gene adenine/cytosine(1166) polymorphism is not associated with mitral valve prolapse syndrome in Taiwan Chinese	Chou, HT; Shi, YR; Wu, JY; Tsai, FJ
中國醫藥大學	2002	The proline form of p53 codon 72 polymorphism is associated with endometriosis	Chang, CC; Hsieh, YY; Tsai, FJ; Tsai, CH; Tsai, HD; Lin, CC
中國醫藥大學	2002	Urokinase gene 3 '-UTR T/C polymorphism is associated with urolithiasis	Tsai, FJ; Lin, CC; Lu, HF; Chen, HY; Chen, WC
中國醫藥大學	2002	Urokinase gene 3 '-UTR T/C polymorphism is associated with urolithiasis	Tsai, FJ; Lin, CC; Lu, HF; Chen, HY; Chen, WC
中國醫藥大學	2002	A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tarda	Shi, YR; Lee, CC; Hsu, YA; Wang, CH; Tsai, FJ
中國醫藥大學	2002	A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tarda	Shi, YR; Lee, CC; Hsu, YA; Wang, CH; Tsai, FJ
中國醫藥大學	2002	Interleukin-1 receptor antagonist gene polymorphism in Chinese patients with systemic lupus erythematosus	Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學	2002	Interleukin-1 receptor antagonist gene polymorphism in Chinese patients with systemic lupus erythematosus	Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學	2002	Distributions of p53 codon 72 polymorphism in primary open angle glaucoma	Lin, HJ; Chen, WC; Tsai, FJ; Tsai, SW
中國醫藥大學	2002	Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method	Shi, YR; Hsieh, KS; Wu, JY; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學	2002	No association of vitamin D receptor gene start codon Fok I Polymorphisms in Chinese patients with systemic lupus erythematosus	Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學	2002	Lack of association of interleukin-1 beta gene polymorphisms in Chinese patients with systemic lupus erythematosus	Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學	2002	Mutation analysis of thyroid peroxidase gene in Chinese patients with total iodide organification defect: Identification of five novel mutations	Wu, JY; Shu, SG; Yang, CF; Lee, CC; Tsai, FJ
中國醫藥大學	2002	Association of vitamin D receptor gene BsmI polymorphisms in Chinese patients with systemic lupus erythematosus	Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學	2002	Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學	2002	Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學	2002	Prognostic significance of the proline form of p53 codon 72 polymorphism in nasopharyngeal carcinoma	Tsai, MH; Lin, CD; Hsieh, YY; Chang, FCC; Tsai, FJ; Chen, WC; Tsai, CH
中國醫藥大學	2002	Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學	2002	Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學	2002	Turner syndrome with pseudodicentric Y chromosome mosaicism	Hsieh, YY; Lin, WC; Chang, CC; Tsai, FJ; Yu, MT; Tsai, HD; Tsai, CH
中國醫藥大學	2002	Turner syndrome with pseudodicentric Y chromosome mosaicism	Hsieh, YY; Lin, WC; Chang, CC; Tsai, FJ; Yu, MT; Tsai, HD; Tsai, CH
中國醫藥大學	2002	p21 gene codon 31 polymorphism is associated with bladder cancer	Chen, WC; Wu, HC; Hsu, CD; Chen, HY; Tsai, FJ
中國醫藥大學	2002	Relation of vitamin D receptor FokI start codon polymorphism. to bone mineral density and occurrence of osteoporosis in postmenopausal women in Taiwan	Chen, HY; Chen, WC; Hsu, CD; Tsai, FJ; Tsai, CH
中國醫藥大學	2002	Molecular analysis of thiopurine S-methyltransferase alleles in South-east Asian populations	Chang, JG; Lee, LS; Chen, CM; Shih, MC; Wu, MC; Tsai, FJ; Liang, DC
中國醫藥大學	2002	Unstable Hb Perth in a Taiwanese subject: A T -> C substitution at codon 32 of the beta-globin gene creates an MspI site	Chang, JG; Liu, HC; Shih, MC; Liu, SC; Chan, WL; Tsai, FJ
中國醫藥大學	2002	Unstable Hb Perth in a Taiwanese subject: A T -> C substitution at codon 32 of the beta-globin gene creates an MspI site	Chang, JG; Liu, HC; Shih, MC; Liu, SC; Chan, WL; Tsai, FJ
中國醫藥大學	2002	Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan	Shi, YR; Wu, JY; Hsu, YA; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學	2002	Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan	Shi, YR; Wu, JY; Hsu, YA; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學	2002	Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers	Lin, WD; Wu, JY; Tsai, FJ; Gau, MT; Lee, CC
中國醫藥大學	2002	Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers	Lin, WD; Wu, JY; Tsai, FJ; Gau, MT; Lee, CC
中國醫藥大學	2002	The voltage-gated potassium channel KCNQ2 in Taiwanese children with febrile convulsions	Chou, IC; Tsai, FJ; Huang, CC; Lin, CC; Tsai, CH
中國醫藥大學	2002	Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method	Shi, YR; Hsieh, KS; Wu, JY; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學	2002	Prognostic significance of the proline form of p53 codon 72 polymorphism in nasopharyngeal carcinoma	Tsai, MH; Lin, CD; Hsieh, YY; Chang, FCC; Tsai, FJ; Chen, WC; Tsai, CH

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