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机构	日期	题名	作者
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	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	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	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	Hydrops foetalis caused by anti-Mur in first pregnancy - a case report	Wu, KH; Chang, JG; Lin, M; Shih, MC; Lin, HC; Lee, CC; Peng, CT; Tsai, CH
中國醫藥大學	2002	Hydrops foetalis caused by anti-Mur in first pregnancy - a case report	Wu, KH; Chang, JG; Lin, M; Shih, MC; Lin, HC; Lee, CC; Peng, CT; Tsai, CH
中國醫藥大學	2002	Environmental risk factors of young onset Parkinson's disease: a case-control study	Tsai, CH; Lo, SK; See, LC; Chen, HZ; Chen, RS; Weng, YH; Chang, FC; Lu, CS
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
中山醫學大學	2001	The correlation between alteration of p16 gene and clinical status in oral squamous cell carcinoma.	Tsai, CH; Yang, CC; Chou, LS; Chou, MY
中山醫學大學	2001	The correlation between alteration of p16 gene and clinical status in oral squamous cell carcinoma.	Tsai, CH; Yang, CC; Chou, LS; Chou, MY
中國醫藥大學	2001	Androgen receptor trinucleotide polymorphism in endometriosis	Hsieh, YY; Chang, CC; Tsai, FJ; Wu, JY; Tsai, CH; Tsai, HD
中國醫藥大學	2001	Further evidence that fibroblast growth factor receptor 2 mutations cause Antley-Bixler syndrome	Tsai, FJ; Wu, JY; Yang, CF; Tsai, CH
中國醫藥大學	2001	Relation of polymorphism in the promotor region for the human osteocalcin gene to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan	Chen, HY; Tsai, HD; Chen, WC; Wu, JY; Tsai, FJ; Tsai, CH
中國醫藥大學	2001	Polymorphisms for interleukin-1 beta (IL-1 beta)-511 promoter, IL-1 beta exon 5, and IL-1 receptor antagonist: Nonassociation with endometriosis	Hsieh, YY; Chang, CC; Tsai, FJ; Wu, JY; Shi, YR; Tsai, HD; Tsai, CH
中國醫藥大學	2001	p21 gene codon 31 arginine/serine polymorphism: Non-association with endometriosis	Hsieh, YY; Tsai, FJ; Chang, CC; Chen, WC; Tsai, CH; Tsai, HD; Lin, CC
中國醫藥大學	2001	Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients	Tsai, FJ; Yang, CF; Wu, JY; Tsai, CH; Lee, CC
中國醫藥大學	2001	Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Lee, CC; Lin, WD
中國醫藥大學	2001	Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Lee, CC; Lin, WD
中國醫藥大學	2001	Leukemia inhibitory factor decreases the arylamine N-acetyltransferase activity in human cumulus granulosa cells	Chang, CC; Hsieh, YY; Chung, JG; Tsai, HD; Tsai, CH
中國醫藥大學	2001	Kinetics of acetyl coenzyme A: Arylamine N-acetyltransferase from human cumulus cells	Chang, CC; Hsieh, YY; Chung, JG; Tsai, HD; Tsai, CH
中國醫藥大學	2001	Kinetics of acetyl coenzyme A: Arylamine N-acetyltransferase from human cumulus cells	Chang, CC; Hsieh, YY; Chung, JG; Tsai, HD; Tsai, CH
中國醫藥大學	2001	Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele	Hsieh, YY; Wu, JY; Chang, CC; Tsai, FJ; Lee, CC; Tsai, HD; Tsai, CH
中國醫藥大學	2001	Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele	Hsieh, YY; Wu, JY; Chang, CC; Tsai, FJ; Lee, CC; Tsai, HD; Tsai, CH
中國醫藥大學	2001	Longitudinal survey of blood flow at three different locations in the middle cerebral artery in normal fetuses	Hsieh, YY; Chang, CC; Tsai, HD; Tsai, CH
中國醫藥大學	2001	Relation of BsmI vitamin D receptor gene polymorphism to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan	Chen, HY; Chen, WC; Hsu, CD; Tsai, FJ; Tsai, CH; Li, CW
中國醫藥大學	2001	Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation	Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH
中國醫藥大學	2001	Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation	Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH
中國醫藥大學	2001	Molecular analysis of SMN, NAIP and P44 genes of SMA patients and their families	Tsai, CH; Jong, YJ; Hu, CJ; Chen, CM; Shih, MC; Chang, CP; Chang, JG
中國醫藥大學	2001	Molecular analysis of SMN, NAIP and P44 genes of SMA patients and their families	Tsai, CH; Jong, YJ; Hu, CJ; Chen, CM; Shih, MC; Chang, CP; Chang, JG
中國醫藥大學	2001	Treatment of spinal muscular atrophy by sodium butyrate	Chang, JG; Hsieh-Li, HM; Jong, YJ; Wang, NM; Tsai, CH; Li, H
中國醫藥大學	2001	Treatment of spinal muscular atrophy by sodium butyrate	Chang, JG; Hsieh-Li, HM; Jong, YJ; Wang, NM; Tsai, CH; Li, H
中國醫藥大學	2001	Reversal caused by n-butylidenephthalide from the deficits of inhibitory avoidance performance in rats	Hsieh, MT; Wu, CR; Lin, LW; Hsieh, CC; Tsai, CH
中國醫藥大學	2001	Relation of the estrogen receptor alpha gene microsatellite polymorphism to bone mineral density and the susceptibility to osteoporosis in postmenopausal Chinese women in Taiwan	Chen, HY; Chen, WC; Tsai, HD; Hsu, CD; Tsai, FJ; Tsai, CH
中國醫藥大學	2001	Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients	Tsai, FJ; Yang, CF; Wu, JY; Tsai, CH; Lee, CC
中國醫藥大學	2001	Longitudinal survey of blood flow at three different locations in the middle cerebral artery in normal fetuses	Hsieh, YY; Chang, CC; Tsai, HD; Tsai, CH
中國醫藥大學	2001	Effects of paeoniflorin on the formalin-induced nociceptive behaviour in mice	Tsai, HY; Lin, YT; Tsai, CH; Chen, YF
國家衛生研究院	2000-09-30	Identification and characterization of a structural protein of hepatitis B virus: A polymerase and surface fusion protein encoded by a spliced RNA	Huang, HL; Jeng, KS; Hu, CP; Tsai, CH; Lo, SJ; Chang, CM
中國醫藥大學	2000	Mutation analysis of type 2 Gaucher disease in Taiwan Chinese and identification of two novel mutations.	Tsai, FJ; Wu, JY; Lin, SP; Chang, JG; Lee, CC; Tsai, CH
中國醫藥大學	2000	Molecular analysis of syndromic congenital heart disease by using short tandem-repeat polymorphic markers.	Shi, YR; Hsieh, KS; Wu, JY; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學	2000	Treatment of spinal muscular atrophy by compound S.	Chang, J; Lee, H; HsiehLi, HM; Jong, YJ; Wang, NM; Tsai, CH
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	Outbreak investigation of nosocomial Enterobacter cloacae bacteraemia in a neonatal intensive care unit	Yu, WL; Cheng, HS; Lin, HC; Peng, CT; Tsai, CH
中國醫藥大學	2000	Longitudinal survey of fetal ventricular ejection and shortening fraction throughout pregnancy	Hsieh, YY; Chang, FCC; Tsai, HD; Tsai, CH
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

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