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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

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