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Showing items 597376-597400 of 2314428 (92578 Page(s) Totally)
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| 臺大學術典藏 |
2018-09-10T08:05:14Z |
Mutation analysis and characterization of alternative splice variants of the Wilson disease gene ATP7B
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Wan, L.;Tsai, C.-H.;Hsu, C.-M.;Huang, C.-C.;Yang, C.-C.;Liao, C.-C.;Wu, C.-C.;Hsu, Y.-A.;Lee, C.-C.;Liu, S.-C.;Lin, W.-D.;Tsai, F.-J.; Chih-Chao Yang |
| 亞洲大學 |
2010-11 |
Mutation analysis and characterization of alternative splice variants of the Wilson disease gene ATP7B.
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萬磊;Wan, Lei;Tsai, FJ |
| 中國醫藥大學 |
1998 |
Mutation analysis in fibroblast growth factor receptor genes: Chinese data
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Lin, SP; Tsai, FJ; Wu, JY; Peng, CT; Tsai, CH |
| 國立成功大學 |
2001-06 |
Mutation analysis in the family of a Taiwanese boy with with epidermolysis bullosa simplex Dowling-Meara
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Ning, C. C.; Chao, Sheau-Chiou; Uitto, J; Shieh, C. C.; Lee, Julia Yu-Yun |
| 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 |
| 中國醫藥大學 |
2001-12 |
Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation
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林瑋德(Wei-De Lin); 鄔哲源(Wu,Jer-Yuarn); 徐秀寶; 蔡輔仁(Tsai,Fuu-Jen)*; 李正淳(Lee,Chun-Cheng); 蔡長海 |
| 中國醫藥大學 |
2001 |
Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation
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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
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Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH |
| 國家衛生研究院 |
2008-02 |
Mutation analysis of adenosine A2a receptor gene and interaction study with dopamine D2 receptor gene in schizophrenia
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Luu, SU; Liao, HM; Hung, TW; Liu, BY; Cheng, MC; Liao, DL; Chen, SJ; Chen, CH |
| 臺北醫學大學 |
2005 |
MUTATION ANALYSIS OF ANDROGEN RECEPTOR GENE IN TAIWAN PROSTATE CANCER PATIENTS
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陳冠州; Chen KC; Cheng CJ; Yan JH; Peng CC; Chiang HS; Hsieh HM |
| 國立成功大學 |
2002-04 |
Mutation analysis of ATP2CI gene in Taiwanese patients with Hailey-Hailey disease
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Chao, Sheau-Chiou; Tsai, Ya-Ming; Yang, Mei-Hui |
| 義守大學 |
2000-04 |
Mutation analysis of BCL 10 in acute myeloid leukaemia
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Liu Ta-Chih;Lin Pai-Mei;Chang Jan-Gowth;Lee Jing-Ping;Chen Tyen-Po;Sue Yu-Chieh;Lin Sheng-Fung |
| 中國醫藥大學 |
2000 |
Mutation analysis of BCL 10 in acute myeloid leukaemia
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Liu, TC; Lin, PM; Chang, JG; Lee, JP; Chen, TP; Sue, YC; Lin, SF |
| 中國醫藥大學 |
1998 |
Mutation analysis of Chinese patients with Wilson disease
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Tsai, FJ; Wu, JY; Chang, JG; Lin, SP; Peng, CT; Tsai, CH |
| 中國醫藥大學 |
2001 |
Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients
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Tsai, FJ; Yang, CF; Wu, JY; Tsai, CH; Lee, CC |
| 中國醫藥大學 |
2001 |
Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients
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Tsai, FJ; Yang, CF; Wu, JY; Tsai, CH; Lee, CC |
| 亞洲大學 |
2006-02 |
Mutation Analysis of Crouzon Syndrome in Taiwanese Patients
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Chin-Ping Chang;Lei Wan;Chang-Hai Tsai;Cheng-Chun Lee;Fuu-Jen Tsai |
| 中國醫藥大學 |
2006-02 |
Mutation Analysis of Crouzon Syndrome in Taiwanese Patients
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張金萍(Chin-Ping Chang);萬磊(Lei Wan);蔡長海(Chang-Hai Tsai);(Cheng-Chun Lee);蔡輔仁(Fuu-Jen Tsai)* |
| 中國醫藥大學 |
2003 |
Mutation analysis of CTNNB1 (beta-catenin) and AXINI, the components of Wnt pathway, in cervical carcinomas
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Su, TH; Chang, JG; Yeh, KT; Lin, TH; Lee, TP; Chen, JC; Lin, CC |
| 中國醫藥大學 |
2003 |
Mutation analysis of CTNNB1 (beta-catenin) and AXINI, the components of Wnt pathway, in cervical carcinomas
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Su, TH; Chang, JG; Yeh, KT; Lin, TH; Lee, TP; Chen, JC; Lin, CC |
| 國家衛生研究院 |
2006-10 |
Mutation analysis of DARPP-32 as a candidate gene for schizophrenia
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Li, CH; Liao, HM; Hung, TW; Chen, CH |
| 臺大學術典藏 |
2020-03-05T03:20:31Z |
Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan
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Lin Y.-C.;Lai H.-S.;Wen-Ming Hsu;Lee P.-I.;Chen H.-L.;Chang M.-H.; Lin Y.-C.; Lai H.-S.; WEN-MING HSU; Lee P.-I.; Chen H.-L.; Chang M.-H. |
| 臺大學術典藏 |
2018-09-10T07:10:02Z |
Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan
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Lin, Y.-C. and Lai, H.-S. and Hsu, W.-M. and Lee, P.-I. and Chen, H.-L. and Chang, M.-H.; 林裕誠;賴鴻緒;許文明;李秉穎;陳慧玲;張美惠; LIN, YU-CHENG;LAI, HONG-SHIEE;HSU, WEN- MING;LEE, PING-ING;CHEN, HUEY-LING;CHANG, MEI-HWEI; PING-ING LEE; WEN-MING HSU; MEI-HWEI CHANG; HONG-SHIEE LAI; LIN, YU-CHENG; LAI, HONG-SHIEE; HSU, WEN- MING; LEE, PING-ING; CHEN, HUEY-LING; CHANG, MEI-HWEI |
| 臺大學術典藏 |
2020-02-24T05:13:25Z |
Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan
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Lin Y.-C.; HONG-SHIEE LAI; Hsu W.-M.; Lee P.-I.; Chen H.-L.; Chang M.-H. |
| 臺大學術典藏 |
2021-01-04T07:36:07Z |
Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan
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Chen H.-L.; MEI-HWEI CHANG; Lee P.-I.; Hsu W.-M.; Lin Y.-C.; Lai H.-S. |
Showing items 597376-597400 of 2314428 (92578 Page(s) Totally)
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