| 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 |
| 義守大學 |
2000-04 |
Mutation analysis of PTEN/MMAC1 in acute myeloid leukemia
|
Ta-Chih Liu;Pai-Mei Lin;Jan-Gowth Chang;Jing-Ping Lee;Tyen-Po Chen;Sheng-Fung Lin |
| 中國醫藥大學 |
2000 |
Mutation analysis of PTEN/MMAC1 in acute myeloid leukemia
|
Liu, TC; Lin, PM; Chang, JG; Lee, JP; Chen, TP; Lin, SF |
| 中國醫藥大學 |
2000 |
Mutation analysis of PTEN/MMAC1 in acute myeloid leukemia
|
Liu, TC; Lin, PM; Chang, JG; Lee, JP; Chen, TP; Lin, SF |
