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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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???jsp.browse.items-by-title.jump??? [ ???jsp.browse.general.jump2chinese??? ] [ ???jsp.browse.general.jump2numbers??? ] [ A B C D E F G H I J K L M N O P Q R S T U V W X Y Z ]
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Institution Date Title Author
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.
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 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.

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