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Institution Date Title Author
義守大學 2000-04 Mutation analysis of BCL 10 in acute myeloid leukaemia 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 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 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 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 Tsai, FJ; Yang, CF; Wu, JY; Tsai, CH; Lee, CC
亞洲大學 2006-02 Mutation Analysis of Crouzon Syndrome in Taiwanese Patients 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 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 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 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 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 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.
國立臺灣大學 2008 Mutation Analysis of Endothelin-B Receptor Gene in Patients with Hirschsprung Disease in Taiwan 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
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 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 Lin Y.-C.; HONG-SHIEE LAI; Hsu W.-M.; Lee P.-I.; Chen H.-L.; Chang M.-H.
臺大學術典藏 2020-03-10T03:30:32Z Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan Hsu W.-M.; Lee P.-I.; HUEY-LING CHEN; Chang M.-H.; Lai H.-S.; Lin Y.-C.; Chang M.-H.;HUEY-LING CHEN;Lee P.-I.;Hsu W.-M.;Lai H.-S.;Lin Y.-C.
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 Chen H.-L.; MEI-HWEI CHANG; Lee P.-I.; Hsu W.-M.; Lin Y.-C.; Lai H.-S.
臺大學術典藏 2008 Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan Lin Y.-C.;Lai H.-S.;Hsu W.-M.;Ping-Ing Lee;Chen H.-L.;Chang M.-H.; Lin Y.-C.; Lai H.-S.; Hsu W.-M.; PING-ING LEE; Chen H.-L.; Chang M.-H.
亞洲大學 2006-05 Mutation analysis of Gaucher disease patients in Taiwan: high prevalence of the RecNciI and L444P mutations Lei Wan;Hsu CM;Chang-Hai Tsai;Lee,Chun-Cheng;Hwu WL;Tsai,Fuu-Jen
國立臺灣大學 2006 Mutation Analysis of Gaucher Disease Patients in Taiwan: High Prevalence of the Recncii and L444p Mutations 許欽木; 蔡長梅; 李正淳; 胡務亮; 蔡輔仁; HSU, CHIN-MOO; TSAI, C-H; LEE, CHENG-CHUN; HWU, WUH-LIANG; TSAI, FUU-JEN
中國醫藥大學 2006-05 Mutation analysis of Gaucher disease patients in Taiwan: high prevalence of the RecNciI and L444P mutations 萬磊(Lei Wan); 許欽木(Hsu CM); 蔡長海; 李正淳(Lee,Chun-Cheng); 胡務亮(Hwu WL); 蔡輔仁(Tsai,Fuu-Jen)*
臺大學術典藏 2020-12-16T02:26:04Z Mutation analysis of Gaucher disease patients in Taiwan: High prevalence of the RecNciI and L444P mutations Wan L.;Hsu C.-M.;Tsai C.-H.;Lee C.-C.;Wuh-Liang Hwu;Tsai F.-J.; Wan L.; Hsu C.-M.; Tsai C.-H.; Lee C.-C.; WUH-LIANG HWU; Tsai F.-J.
中國醫藥大學 2000 Mutation Analysis of Human LEFTY A and LEFTY B Genes in Children with Ivemark Syndrome 陳汶吉(Chen Wen-Chi); 蔡輔仁(Fuu-Jen Tsai); 鄔哲源; 施怡如(Shi YR); 吳錫金(Hsi-Chin Wu)
臺大學術典藏 2018-09-10T09:48:53Z Mutation analysis of papillary tubal hyperplasia associated with ovarian atypical proliferative serous tumor and low-grade serous carcinoma Huang, W.-C. and Tsai, C.-C. and Wei, M.-C. and Kuo, K.-T.; KUAN-TING KUO
臺大學術典藏 2020-03-07T06:42:13Z Mutation analysis of papillary tubal hyperplasia associated with ovarian atypical proliferative serous tumor and low-grade serous carcinoma Huang W.-C.; Tsai C.-C.; Wei M.-C.; KUAN-TING KUO
臺大學術典藏 2013 Mutation analysis of papillary tubal hyperplasia associated with ovarian atypical proliferative serous tumor and low-grade serous carcinoma Huang W.-C.; Tsai C.-C.; Wei M.-C.; KUAN-TING KUO

Showing items 603086-603110 of 2348419  (93937 Page(s) Totally)
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