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显示项目 41-61 / 61 (共3页)
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机构 日期 题名 作者
國立臺灣大學 2006-06 Evaluation of RGS4 as a Candidate Gene for Schizophrenia Liu, Yu-Li; Fann, Cathy Shen-Jang; Liu, Chih-Min; Wu, Jer-Yuarn; Hung, Shuen-Iu; Chan, Hung-Yu; Chen, Jiahn-Jyh; Lin, Chin-Yu; Liu, Shih-Kai; Hsieh, Ming H.; Hwang, Tzung-Jeng; OuYang, Wen-Chen; Chen, Chun-Ying; Lin, Jin-Jia; Chou, Frank Huang-Chih; Chueh, Ching-Mo; Liu, Wei-Ming; Tsuang, Ming-Min; Faraon, Stephen V.
國立臺灣大學 2006-01 Absence of Significant Associations between Four AKT1 SNP Markers and Schizophrenia in Taiwanese Population Liu, Yu-Li; Fann, Cathy Shen-Jang; Liu, Chih-Min; Wu, Jer-Yuarn; Hung, Shuen-Iu; Chan, Hung-Yu; Chen, Jiahn-Jyh; Pan, Chia-Ching; Hwu, Hai-Gwo
國立臺灣大學 2006 No association of G72 and d-amino acid oxidase genes with schizophrenia Liu, Yu-Li; Fann, Cathy Shen-Jang; Liu, Chih-Min; Chang, Chien Ching; Wu, Jer-Yuarn; Hung, Shuen-Iu; Liu, Shih-Kai; Hsieh, Ming H.; Hwang, Tzung-Jeng; Chan, Hung-Yu; Chen, Jiahn-Jyh; Faraone, Stephen V.; Tsuang, Ming T.; Chen, Wei J.; Hwu, Hai-Gwo
國立臺灣大學 2006 Absence of significant associations between four AKT1 SNP markers and schizophrenia in the Taiwanese population Liu, Yu-Li; Fann, Cathy Shen-Jang; Liu, Chih-Min; Wu, Jer-Yuarn; Hung, Shuen-Iu; Chan, Hung-Yu; Chen, Jiahn-Jyh; Pan, Chia-Ching; Liu, Shih-Kai; Hsieh, Ming H.; Hwang, Tzung-Jeng; OuYang, Wen-Chen; Chen, Chun-Ying; Lin, Jin-Jia; Chou, Frank Huang-Chih; Chueh, Ching-Mo; Liu, Wei-Ming; Tsuang, Ming-Ming; Faraone, Stephen V.; Tsuang, Ming T.; Chen, Wei J.; Hwu, Hai-Gwo
國立臺灣大學 2005 Mapping of Psoriasis to 17q Terminus 胡務亮; 范盛娟; 蔡呈芳; 簡穎秀; 蔣書娟; 鄔哲源; 陳垣崇; HWU, WUH-LIANG; FANN, CATHY SHENG-JIUAN; TSAI, TSEN-FANG; CHIEN, YIN-HSIU; CHIANG, SHU-CHUAN; WU, JER-YUARN; CHEN, YUAN-TSONG
國立臺灣大學 2005 Kif21a Gene C.2860c>T Mutation in Congenital Fibrosis of Extraocular Muscles Type 1 and 3 林隆光; 簡穎秀; 鄔哲源; 王藹侯; 蔣書娟; 胡務亮; LIN, LUKE LONG-KUANG; CHIEN, YIN-HSIU; WU, JER-YUARN; WANG, AI-HOU; CHIANG, SHU-CHUAN; HWU, WUH-LIANG
亞洲大學 2004-07 Isovaleric acidemia diagnosed promptly by tandem mass spectrometry: report of one case Chang-Ching Wei;Wei-De Lin;Tsai,Fuu-Jen;Wu,Jer-Yuarn;Peng,Ching-Tien
國立臺灣大學 2004 Association Analysis of Nine Candidate Genes of Schizophrenia of Rgs4, Mrds1, Dtnbp1, Tnf-a, Notch4, Ppp3cc, Nrg1, Daao, and G72 in Taiwanese Family Sample 胡海國; 劉智民; 范盛娟; 劉玉麗; 林錦瑜; 陳為堅; 歐陽文貞; 詹宏裕; 鄔哲源; HWU, HAI-GWO; LIU, CHIH-MIN; FANN, CATHY SHENG-JIUAN; LIU, YU-LI; LIN, CHIN-YU; CHEN, WEI-JANE; OUYANG, WEN-CHEN; CHAN, HUNG-YU; WU, JER-YUARN
亞洲大學 2003-08 Association of the neuronal nicotinic acetylcholine receptor subunit alpha4 polymorphisms with febrile convulsions I-Ching Chou;Cheng-Chun Lee;Huang CC;Wu,Jer-Yuarn;Tsai JJ;Chang-Hai Tsai;Fuu-Jen Tsai
國立成功大學 2003-08 Association of the neuronal nicotinic acetylcholine receptor subunit alpha 4 polymorphisms with febrile convulsions Chou, I-Ching; Lee, Cheng-Chun; Huang, Chao-Ching; Wu, Jer-Yuarn; Tsai, Jeffrey J. P.; Tsai, Chang-Hai; Tsai, Fuu-Jen
亞洲大學 2003-05 Genetic analysis of chromosome 22q11.2 markers in congenital heart disease Shi YR;Hsieh KS;Wu,Jer-Yuarn;Lee,Chun-Cheng;YU MT;Jeng-Sheng Chang;Fuu-Jen Tsai;Chang-Hai Tsai
亞洲大學 2002-02 Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots Lai,Chien-Chen;Tsai,Fuu-Jen;Wu,Jer-Yuarn;Wei-De Lin;Lee,Chun-Cheng;Chang-Hai Tsai
亞洲大學 2002-01 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,Chien-Chen;Chang-Hai Tsai;Tsai,Fuu-Jen;Wu,Jer-Yuarn;Wei-De Lin;Lee,Chun-Cheng
亞洲大學 2002-01 Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method Shi YR;Hsieh KS;Wu,Jer-Yuarn;Cheng-Chun Lee;Chang-Hai Tsai;Fuu-Jen Tsai
亞洲大學 2002 Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan Shi YR;Wu,Jer-Yuarn;Hsu YA;Cheng-Chun Lee;Chang-Hai Tsai;Fuu-Jen Tsai
亞洲大學 2001-12 Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation Wei-De Lin;Wu,Jer-Yuarn;Tsai,Fuu-Jen;Lee,Chun-Cheng;Chang-Hai Tsai
亞洲大學 2001-11 Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots Lai,Chien-Chen;Chang-Hai Tsai;Tsai,Fuu-Jen;Wu,Jer-Yuarn;Wei-De Lin;Lee,Chun-Cheng
亞洲大學 2001-07 A pilot study of neonatal screening by electrospray ionization tandem mass spectrometry in Taiwan Wei-De Lin;Wu,Jer-Yuarn;Lai,Chien-Chen;Tsai,Fuu-Jen;Chang-Hai Tsai
亞洲大學 2001-05 Pitfalls of PCR-based genotyping in patients with 21-hydroxylase deficiency Chang-Hai Tsai;Wei-De Lin;Tsai,Fuu-Jen;Peng,Ching-Tien;Wu,Jer-Yuarn
亞洲大學 2001 Relation of polymorphism in the region of human osteocalcin gene to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan Huey-Yi Chen;Tsai HD;Chen Wen-Chi;Wu,Jer-Yuarn;Fuu-Jen Tsai;Chang-Hai Tsai
亞洲大學 2000-10 A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia Tsai,Fuu-Jen;Wu,Jer-Yuarn;Wei-De Lin;Chang-Hai Tsai

显示项目 41-61 / 61 (共3页)
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