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教育部委託研究計畫      計畫執行:國立臺灣大學圖書館
 
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機構 日期 題名 作者
亞洲大學 2020-01-20 Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects Ch, Chih-Ping;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Che, Shin-Wen;Chen, Shin-Wen;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Wu, Fang-Tzu;Wu, Fang-Tzu;Chen, Wen-Lin;Chen, Wen-Lin;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen
亞洲大學 2020-01-20 Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication Ch, Chih-Ping;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;Wu, Fang-Tzu;Wu, Fang-Tzu;Chen, Wen-Lin;Chen, Wen-Lin;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen
亞洲大學 2019-11 Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound 陳持平;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;Wang, Wayseen;Wang, Wayseen;Lee, Chen-Chi;Lee, Chen-Chi
國立臺灣師範大學 2016-07-22T06:03:50Z Effects of tobacco exposure on perinatal suicidal ideation, depression, and anxiety Weng, Shu-Chuan; Huang, Jian-Pei; Huang, Ya-Li; Lee, Tony S; Chen, Yi-Hua
國立成功大學 2016-06 Efficacy of Femarelle for the treatment of climacteric syndrome in postmenopausal women: An open label trial Chen, Fang-Ping; Chang, Chee Jen; Chao, An-Shine; Huang, Hong-Yuan; Huang, Jian-Pei; Wu, Meng-Hsing; Tsai, Ching-Chou; Kung, Fu-Tsai; Chang, Ching-Wen; Tsai, Yung-Chieh
嘉南藥理大學 2016-06 Efficacy of Femarelle for the treatment of climacteric syndrome in postmenopausal women: An open label trial Chen, Fang-Ping; Chang, Chee Jen; Chao, An-Shine; Huang, Hong-Yuan; Huang, Jian-Pei; Wu, Meng-Hsing; Tsai, Ching-Chou; Kung, Fu-Tsai; Chang, Ching-Wen; Tsai, Yung-Chieh
亞洲大學 201310 Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review 陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Su, Yi-Ning;Su, Yi-Ning;Hua, Jian-Pei;Huang, Jian-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Ch, Shun-Ping;Chang, Shun-Ping;Chen, Li-Feng;Chen, Li-Feng;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen
亞洲大學 201309 Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review 陳持平;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen
亞洲大學 201309 Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes 陳持平;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen
亞洲大學 2013-10 Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review 陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Su, Yi-Ning;Su, Yi-Ning;Hua, Jian-Pei;Huang, Jian-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Ch, Shun-Ping;Chang, Shun-Ping;Chen, Li-Feng;Chen, Li-Feng;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen

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