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"wei de lin"
Showing items 1-14 of 14 (1 Page(s) Totally)
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| 中山醫學大學 |
2021-05-24 |
Effects of Acrylamide-Induced Vasorelaxation and Neuromuscular Blockage: A Rodent Study
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Wei-De Lin;Chu-Chyn Ou;Shih-Hao Hsiao;Chih-Han Chang;Fuu-Jen Tsai ;Jiunn-Wang Liao;Yng-Tay Chen |
| 亞洲大學 |
2007-09 |
Human Gene Mutations. Gene symbol: EXT2. Disease: Exostoses (multiple) 2
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Wei-De Lin;Chang-Hai Tsai;Chih-Ping Chen;Fuu-Jen Tsai |
| 亞洲大學 |
2007-05 |
Rapid screening assay of trimethylaminuria in urine with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
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Wei-Yi Hsu;Wan-Yu Lo;Chien-Chen Lai;Fuu-Jen Tsai;Chang-Hai Tsai;Yuhsin Tsai;Wei-De Lin;Mei-Chyn Chao |
| 亞洲大學 |
2006-11 |
Penil length of noormal boys in Taiwan
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Wei-De Lin;Chang-Hai Tsai;Da-Tian Bau;Tsai,Fuu-Jen |
| 亞洲大學 |
2006-11 |
Holocarboxylase synthetase deficiency: a case report and mutatio detection
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Wei-De Lin;Hsin-Chen Lin;Chang-Hai Tsai;Tsai,Fuu-Jen |
| 亞洲大學 |
2006 |
Holocarboxylase synthetase deficiency: Report of one case
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I-Ching Chou;Chung-Hsing Wang;Wei-De Lin;Hsin-Chen Lin;Chang-Hai Tsai |
| 亞洲大學 |
2004-07 |
Isovaleric acidemia diagnosed promptly by tandem mass spectrometry: report of one case
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Chang-Ching Wei;Wei-De Lin;Tsai,Fuu-Jen;Wu,Jer-Yuarn;Peng,Ching-Tien |
| 亞洲大學 |
2002-02 |
Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots
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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
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Lai,Chien-Chen;Chang-Hai Tsai;Tsai,Fuu-Jen;Wu,Jer-Yuarn;Wei-De Lin;Lee,Chun-Cheng |
| 亞洲大學 |
2001-12 |
Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation
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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
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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
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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
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Chang-Hai Tsai;Wei-De Lin;Tsai,Fuu-Jen;Peng,Ching-Tien;Wu,Jer-Yuarn |
| 亞洲大學 |
2000-10 |
A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia
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Tsai,Fuu-Jen;Wu,Jer-Yuarn;Wei-De Lin;Chang-Hai Tsai |
Showing items 1-14 of 14 (1 Page(s) Totally)
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