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Institution	Date	Title	Author
國立臺灣大學	1996	Identification of a BglI polymorphism of Catechol-O-methyltransferase (COMT) gene, and association study with schizophrenia	Chen, Chia-Hsiang; Lee, Yu-Ru; Liu, Mei-Ying; Wei, Fu-Chuan; Koong, Farn-Jong; Hwu, Hai-Gwo; Hsiao, Kwang-Jen
中國醫藥大學	2008-04-10	Identification Of A C/T Polymorphism In HLA-E 3’UTR Region Associated With Taiwanese Kawasaki Disease Patients	林應如(Ying-Ju Lin); 張正成(Jeng-Sheng Chang)*; (Jer-Yuarn Wu); 萬磊(Lei Wan); 蔡育勳(Yuhsin Tsai); 蔡長海(Chang-Hai Tsai); (Jim Jinn-Chyuan Sheu); 蔡輔仁(Fuu-Jen Tsai)
義守大學	2016-08	Identification of a capsular variant and characterization of capsular acetylation in Klebsiella pneumoniae PLA-associated type K57	Chun-Ru Hsu;Chun-Hsing Liao;Tzu-Lung Lin;Han-Ru Yang;Feng-Ling Yang;Pei-Fang Hsieh;Shih-Hsiung Wu;Jin-Town Wang
國立臺灣大學	2016	Identification of a capsular variant and characterization of capsular acetylation in Klebsiella pneumoniae PLA-associated type K57	Hsu, Chun-Ru; Liao, Chun-Hsing; Lin, Tzu-Lung; Yang, Han-Ru; Yang, Feng-Ling; Hsieh, Pei-Fang; Wu, Shih-Hsiung; Wang, Jin-Town; 林稚容; 王錦堂
臺大學術典藏	2020-02-03T08:43:42Z	Identification of a carboxylesterase associated with resistance to naled in Bactrocera dorsalis (Hendel)	Hsu P.-K.; Huang L.-H.; Geib S.M.; Hsu J.-C.; JU-CHUN HSU
亞洲大學	2019-12	Identification of a case with heterozygous mutations in the FUT1 gene leading to a para-Bombay phenotype	林志隆;余志強;KIONG, ER TZE
國立交通大學	2014-12-08T15:03:48Z	IDENTIFICATION OF A CLASS OF NONLINEAR DETERMINISTIC SYSTEMS WITH APPLICATION TO MANIPULATORS	LIN, SK
亞洲大學	2012-06	Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II	陳持平;Chen, Chih-Ping
中國醫藥大學	2012-06	Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II	陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Fang-Yu Hung);(Schu-Rern Chern);(Jun-Wei Su);(Wayseen Wang)
中國醫藥大學	1999	Identification of a common N540K mutation in 8/18 Taiwanese hypochondroplasia patients: further evidence for genetic heterogeneity	Tsai, FJ; Wu, JY; Tsai, CH; Chang, JG

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