| 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 |
