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"lee chun cheng"的相关文件
显示项目 1-10 / 12 (共2页)
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| 亞洲大學 |
2007-03 |
Disease association of the interleukin-18 promoter polymorphisms in Taiwan Chinese systemic lupus erythematosus patients
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Ying-Ju Lin;Lei Wan;Lee,Chun-Cheng;Chung-Ming Huang;Chang-Hai Tsai;Tsai,Fuu-Jen |
| 亞洲大學 |
2007-01 |
Association of GABRG2 Polymorphisms with Idiopathic Generalized Epilepsy
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I-Ching Chou;Lee,Chun-Cheng;Chang-Hai Tsai;Yuhsin Tsai;Lei Wan;Yu-An Hsu;Tsai-Chung Li;Tsai,Fuu-Jen |
| 亞洲大學 |
2006-06 |
Mutation analysis of Taiwanese Wilson disease patients
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Lei Wan;Chang-Hai Tsai;Yuhsin Tsai;Hsu CM;Lee,Chun-Cheng;Tsai,Fuu-Jen |
| 亞洲大學 |
2006-05 |
Vitamin D receptor gene polymorphisms are associated with risk of Hashimoto's thyroiditis in Chinese patients in Taiwan
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Wei-Yong Lin;Lei Wan;Chang-Hai Tsai;Rong-Sing Chen;Lee,Chun-Cheng;Tsai,Fuu-Jen |
| 亞洲大學 |
2006-05 |
Mutation analysis of Gaucher disease patients in Taiwan: high prevalence of the RecNciI and L444P mutations
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Lei Wan;Hsu CM;Chang-Hai Tsai;Lee,Chun-Cheng;Hwu WL;Tsai,Fuu-Jen |
| 亞洲大學 |
2003-05 |
Genetic analysis of chromosome 22q11.2 markers in congenital heart disease
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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
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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 |
| 國立臺灣大學 |
2002 |
Spin-dependent transport in a two-dimensional GaAs electron gas in a parallel magnetic field
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Cheng, Yu-Ming; Huang, Tsai-Yu; Pao, Chao Han; Lee, Chun-Cheng; Liang, C. -T.; Simmons, M. Y.; Smith, C. G.; Ritchie, D. A.; Pepper, M.; Kim, Gil-Ho; Leem, J. Y. |
| 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 |
显示项目 1-10 / 12 (共2页)
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