English  |  正體中文  |  简体中文  |  2826208  
???header.visitor??? :  31895750    ???header.onlineuser??? :  1514
???header.sponsordeclaration???
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
???ui.leftmenu.abouttair???

???ui.leftmenu.bartitle???

???index.news???

???ui.leftmenu.copyrighttitle???

???ui.leftmenu.link???

"fang js"???jsp.browse.items-by-author.description???

???jsp.browse.items-by-author.back???
???jsp.browse.items-by-author.order1??? ???jsp.browse.items-by-author.order2???

Showing items 1-11 of 11  (1 Page(s) Totally)
1 
View [10|25|50] records per page

Institution Date Title Author
國立交通大學 2014-12-08T15:41:36Z Direct sums of irreducible operators Fang, JS; Jiang, CL; Wu, PY
國立交通大學 2014-12-08T15:17:32Z Path-dependent human identification using a pyroelectric infrared sensor and Fresnel lens arrays Fang, JS; Hao, Q; Brady, DJ; Shankar, M; Guenther, BD; Pitsianis, NP; Hsu, KY
國家衛生研究院 2013-10 Chromosomal abnormalities in patients with autism spectrum disorders from Taiwan Liao, HM;Gau, SSF;Tsai, WC;Fang, JS;Su, YC;Chou, MC;Liu, SK;Chou, WJ;Wu, YY;Chen, CH
國家衛生研究院 2012-08 Identification and characterization of three inherited genomic copy number variations associated with familial schizophrenia Liao, HM;Chao, YL;Huang, AL;Cheng, MC;Chen, YJ;Lee, KF;Fang, JS;Hsu, CH;Chen, CH
國家衛生研究院 2011-05 Clinical and molecular characterization of a transmitted reciprocal translocation t(1;12)(p32.1; q21.3) in a family co-segregating with mental retardation, language delay, and microcephaly Liao, HM;Fang, JS;Chen, YJ;Wu, KL;Lee, KF;Chen, CH
國家衛生研究院 2011-01 Identification of a microdeletion at Xp22.13 in a Taiwanese family presenting with Nance-Horan syndrome Liao, HM;Niu, DM;Chen, YJ;Fang, JS;Chen, SJ;Chen, CH
國家衛生研究院 2010-11 Identification and molecular characterization of two novel chromosomal deletions associated with autism Chien, WH;Gau, SSF;Wu, YY;Huang, YS;Fang, JS;Chen, YJ;Soong, WT;Chiu, YN;Chen, CH
國家衛生研究院 2009-09 Copy number variations and psychiatric disorders Chao, YL;Chien, WH;Liao, HM;Fang, JS;Chen, CH
國家衛生研究院 2009-05 A novel microdeletion at chromosome 2q31.1-31.2 in a three-generation family presenting duplication of great toes with clinodactyly Tsai, LP;Liao, HM;Chen, YJ;Fang, JS;Chen, CH
國家衛生研究院 2008-06 Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion Fang, JS; Lee, KF; Huang, CT; Syu, CL; Yang, KJ; Wang, LH; Liao, DL; Chen, CH
國家衛生研究院 2007-12 Chromosomal Abnormalities and Gene Discovery in Schizophrenia Fang, JS;Chen, CH

Showing items 1-11 of 11  (1 Page(s) Totally)
1 
View [10|25|50] records per page