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Showing items 11-60 of 141  (3 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2022-01-15T00:08:30Z Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14) (q10;q10) Chen, Chih Ping; MING CHEN; Ma, Gwo Chin; Chang, Shun Ping; Chern, Schu Rern; Chen, Shin Wen; Wu, Fang Tzu; Lee, Meng Shan; Wang, Wayseen
臺大學術典藏 2022-01-15T00:08:29Z Editorial: Emerging New Tests and Their Impact Upon the Practice of Reproductive Genetics Leung, Kwok Yin; Borrell, Antoni; Evans, Mark I.; MING CHEN
臺大學術典藏 2022-01-15T00:08:29Z Difficulties of Prenatal Genetic Counseling for a Subsequent Child in a Family With Multiple Genetic Variations Huang, Ting Xuan; Ma, Gwo Chin; MING CHEN; Li, Wen Fang; Shaw, Steven W.
臺大學術典藏 2022-01-15T00:08:21Z Preimplantation genetic diagnosis in hereditary hearing impairment Chen, Hsin Lin; PEI-HSUAN LIN; Chiang, Yu Ting; Huang, Wen Jie; Lin, Chi Fang; Ma, Gwo Chin; Chang, Shun Ping; Fan, Jun Yang; SHIN-YU LIN; CHEN-CHI WU; MING CHEN
臺大學術典藏 2021-09-17T07:57:39Z An Automatic Platform Based on Nanostructured Microfluidic Chip for Isolating and Identification of Circulating Tumor Cells Jou, Hei-Jen; Chou, Li-Yun; WEN-CHUN CHANG; Ho, Hsin-Cheng; Zhang, Wan-Ting; Ling, Pei-Ying; Tsai, Ko-Hsin; Chen, Szu-Hua; Chen, Tze-Ho; Lo, Pei-Hsuan; MING CHEN; Hsu, Heng-Tung
臺大學術典藏 2021-09-14T23:19:14Z Prenatal diagnosis of true fetal mosaicism with small supernumerary marker chromosome derived from chromosome 16 by funipuncture and molecular cytogenetics including chromosome microarray Yao, Tien Yu; Wu, Wan Ju; Law, Kim Seng; Lee, Mei Hui; Chang, Shun Ping; Lee, Dong Jay; Lin, Wen Hsiang; MING CHEN; Ma, Gwo Chin
臺大學術典藏 2021-09-10T07:52:27Z Using next-generation sequencing to redefine BRCAness in triple-negative breast cancer Lin, Po-Han; MING CHEN; TSAI, LI-WEI; Lo, Chiao; Yen, Tzu-Chun; Huang, Thomas Yoyan; Chen, Chih-Kai; Fan, Sheng-Chih; Kuo, Sung-Hsin; Huang, Chiun-Sheng
臺大學術典藏 2021-07-15T05:32:33Z Comparison of genetic profiling between primary tumor and circulating tumor cells captured by microfluidics in epithelial ovarian cancer: Tumor heterogeneity or Allele dropout? Chang, Ting Yu; Chen, Sheng Wen; Lin, Wen Hsiang; Huang, Chung Er; Evans, Mark I.; Chung, I. Fang; Wu, Janne Wha; Ma, Gwo Chin; MING CHEN
臺大學術典藏 2021-07-15T05:32:33Z An automatic platform based on nanostructured microfluidic chip for isolating and identification of circulating tumor cells Jou, Hei Jen; Chou, Li Yun; WEN-CHUN CHANG; Ho, Hsin Cheng; Zhang, Wan Ting; Ling, Pei Ying; Tsai, Ko Hsin; Chen, Szu Hua; Chen, Tze Ho; Lo, Pei Hsuan; MING CHEN; Hsu, Heng Tung
臺大學術典藏 2021-07-15T05:32:33Z Understanding false negative in prenatal testing Evans, Mark I.; MING CHEN; Britt, David W.
臺大學術典藏 2021-03-02T03:44:01Z Preimplantation Genetic Diagnosis of Neurodegenerative Diseases: Review of Methodologies and Report of Our Experience as a Regional Reference Laboratory Liao, Chun-Hua;Chang, Ming-Yuh;Ma, Gwo-Chin;Chang, Shun-Ping;Lin, Chi-Fang;Lin, Wen-Hsiang;Chen, Hsin-Fu;Shee-Uan Chen;Lee, Yi-Chung;Chao, Chi-Chao;Ming Chen;Hsieh, Sung-Tsang; Liao, Chun-Hua; Chang, Ming-Yuh; Ma, Gwo-Chin; Chang, Shun-Ping; Lin, Chi-Fang; Lin, Wen-Hsiang; Chen, Hsin-Fu; SHEE-UAN CHEN; Lee, Yi-Chung; Chao, Chi-Chao; MING CHEN; Hsieh, Sung-Tsang
國立成功大學 2021 Stable Ethosome-like Catanionic Vesicles for Transdermal Hydrophilic Drug Delivery with Predictable Encapsulation Efficiency Wang;Chun-Wei;Chuang;Ming-Chen;Chang;Chieh-Yi;Chang;Chien-Hsiang;Yang;Yu-Min
國立成功大學 2018-10-22 Floating top gate-induced output enhancement of a-InGaZnO thin film transistors under single gate operations Tai;Mao-Chou;Chang;Ting-Chang;Chen;Ming-Chen;Chian;Hsiao-Cheng;Tsao;Yu-Ching;Chien;Yu-Chieh;Wang;Yu-Xuan;Tsai;Yu-Lin;Chen;Jian-Jie;Zhang;Shengdong;Chang;Hsi-Ming
臺大學術典藏 2018-09-10T18:06:25Z The use of low molecular weight heparin reduced the fetal fraction and rendered the cell-free DNA testing for trisomy 21 false negative. Ming Chen; MING CHEN
臺大學術典藏 2018-09-10T18:06:25Z Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9 Chen, C.-P. And Chen, M. And Wang, L.-K. And Chern, S.-R. And Wu, P.-S. And Chen, S.-W. And Lai, S.-T. And Chang, S.-P. And Yang, C.-W. And Pan, C.-W. And Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T18:06:25Z Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions Chen, C.-P. And Chen, M. And Hwu, Y.-M. And Chang, S.-P. And Chen, S.-W. And Lai, S.-T. And Lee, C.-C. And Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T18:06:25Z Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11 Chen, C.-P. And Chen, M. And Wang, P.-T. And Chern, S.-R. And Chen, S.-W. And Lai, S.-T. And Wu, P.-S. And Chang, S.-P. And Pan, C.-W. And Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T18:06:25Z Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2 Chen, C.-P. And Chen, M. And Chang, S.-P. And Hung, F.-Y. And Lee, M.-J. And Chern, S.-R. And Wu, P.-S. And Chen, Y.-N. And Chen, S.-W. And Lee, C.-C. And Town, D.-D. And Chen, W.-L. And Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T18:06:25Z Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21 Chen, C.-P. And Chen, M. And Chern, S.-R. And Chang, S.-P. And Chen, S.-W. And Lai, S.-T. And Chen, W.-L. And Lee, M.-S. And Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T18:06:25Z Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review Chen, C.-P. And Chen, M. And Wu, C.-H. And Lin, C.-J. And Chern, S.-R. And Wu, P.-S. And Chen, Y.-N. And Chen, S.-W. And Chang, S.-P. And Chen, L.-F. And Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T18:06:25Z Species and sex comparisons of karyotype and genome size in two Kurixalus tree frogs (Anura, rhacophoridae) Chang, S.-P. And Ma, G.-C. And Chen, M. And Wu, S.-H.; MING CHEN
臺大學術典藏 2018-09-10T15:38:52Z Low-molecular-weight-heparin can benefit women with recurrent pregnancy loss and sole protein S deficiency: a historical control cohort study from Taiwan Ming Chen; MING CHEN
臺大學術典藏 2018-09-10T15:38:52Z Revelation of 22q11.2 microduplication by cell-free DNA screening and chromosome microarray in a fetus with multiple anomalies. Ming Chen; MING CHEN
臺大學術典藏 2018-09-10T15:38:52Z A pilot proof-of-principle study to compare fresh and vitrified cycle preimplantation genetic screening by chromosome microarray and next generation sequencing Ma, G.-C.;Chen, H.-F.;Yang, Y.-S.;Lin, W.-H.;Tsai, F.-P.;Lin, C.-F.;Chiu, C.;Chen, M.; Ma, Gwo-Chin; MING CHEN; HSIN-FU CHEN; YU-SHIH YANG; Lin, Wen-Hsiang; Tsai, Feng-Po; Lin, Chi-Fang; Chiu, Chi
臺大學術典藏 2018-09-10T15:38:52Z Confined placental mosaicism of double trisomies 9 and 21: discrepancy between non-invasive prenatal testing, chorionic villus sampling and postnatal confirmation Cheng, H.-H.;Ma, G.-C.;Tsai, C.-C.;Wu, W.-J.;Lan, K.-C.;Hsu, T.-Y.;Yang, C.-W.;Chen, M.; MING CHEN
臺大學術典藏 2018-09-10T15:38:52Z De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD Shen, M.-C.;Chen, M.;Ma, G.-C.;Chang, S.-P.;Lin, C.-Y.;Lin, B.-D.;Hsieh, H.-N.; MING CHEN
臺大學術典藏 2018-09-10T15:38:52Z Late onset of large benign ductus arteriosus aneurysm presented with increased nuchal translucency and cystic hygroma at first trimester Down syndrome screening Tsai, H.-D.;Chen, K.;Lee, M.-L.;Lee, C.-H.;Chen, T.-H.;Lin, W.-H.;Chen, M.; MING CHEN
臺大學術典藏 2018-09-10T15:38:52Z Preimplantation genetic diagnosis of hemophilia A Chen, M.;Chang, S.-P.;Ma, G.-C.;Lin, W.-H.;Chen, H.-F.;Chen, S.-U.;Tsai, H.-D.;Tsai, F.-P.;Shen, M.-C.; MING CHEN
臺大學術典藏 2018-09-10T15:38:52Z Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay Chen, C.-P.;Chiang, S.;Wang, K.-L.;Cho, F.-N.;Chen, M.;Chern, S.-R.;Wu, P.-S.;Chen, Y.-N.;Chen, S.-W.;Chang, S.-P.;Chen, W.-L.;Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T15:38:51Z Ultrasonography for prognosis in case of trisomy 14 confined placental mosaicism developing after preimplantation genetic screening Ming Chen; MING CHEN
臺大學術典藏 2018-09-10T15:33:51Z Urorectal septum malformation sequence—Fetal series with the description of a new “intermediate” variant. Time to refine the terminology? Huang, K.-Y.;Kuo, K.-T.;Li, Y.-P.;Chen, M.;Yu, C.-U.;Shih, J.-C.; Huang, Kuan-Ying; MING CHEN; JIN-CHUNG SHIH; Kuo, Kuan-Ting; Li, Yi-Ping; KUAN-TING KUO; Chen, Ming; Yu, Ching-Uen; Shih, Jin-Chung
臺大學術典藏 2018-09-10T15:28:18Z Lessons learned from two missed prenatal cases of hemoglobin Bart’s hydrops fetalis until second trimester despite a nationwide screening program. Ming Chen; MING CHEN
臺大學術典藏 2018-09-10T15:02:34Z Genome-wide normalized score: A novel algorithm to detect fetal trisomy 21 during non-invasive prenatal testing Yeang, C.H.;Ma, G.C.;Hsu, H.W.;Lin, Y.S.;Chang, S.M.;Cheng, P.J.;Chen, C.A.;Ni, Y.H.;Chen, M.; MING CHEN; CHI-AN CHEN
臺大學術典藏 2018-09-10T15:02:34Z Partial trisomy 8 mosaicism not detected by cultured amniotic-fluid cells Tsai, M.-C.;Cheng, H.-Y.;Su, M.-T.;Chen, M.;Kuo, P.-L.; MING CHEN
臺大學術典藏 2018-09-10T15:02:34Z Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry Chen, C.-P.;Chen, M.;Chen, C.-Y.;Chern, S.-R.;Wu, P.-S.;Chang, S.-P.;Kuo, Y.-L.;Chen, W.-L.;Pan, C.-W.;Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T15:02:34Z Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15 Chen, C.-P.;Chen, M.;Su, Y.-N.;Chern, S.-R.;Wu, P.-S.;Chang, S.-P.;Kuo, Y.-L.;Chen, W.-L.;Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T14:57:06Z Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization Chen, M. and Yang, Y.-S. and Shih, J.-C. and Lin, W.-H. and Lee, D.-J. and Lin, Y.-S. and Chou, C.-H. and Cameron, A.D. and Ginsberg, N.A. and Chen, C.-A. and Lee, M.-L. and Ma, G.-C.; MING CHEN; CHI-AN CHEN; JIN-CHUNG SHIH
臺大學術典藏 2018-09-10T09:14:30Z Experimental treatment of bilateral fetal chylothorax using in-utero pleurodesis Yang, Y.-S. and Ma, G.-C. and Shih, J.-C. and Chen, C.-P. and Chou, C.-H. and Yeh, K.-T. and Kuo, S.-J. and Chen, T.-H. and Hwu, W.-L. and Lee, T.-H. and Chen, M.; MING CHEN; YU-SHIH YANG; JIN-CHUNG SHIH; WUH-LIANG HWU
臺大學術典藏 2018-09-10T09:14:30Z Genome-wide gene expression analysis implicates the immune response and lymphangiogenesis in the pathogenesis of fetal chylothorax Yeang, C.-H. and Ma, G.-C. and Shih, J.-C. and Yang, Y.-S. and Chen, C.-P. and Chang, S.-P. and Wu, S.-H. and Liu, C.-S. and Kuo, S.-J. and Chou, H.-C. and Hwu, W.-L. and Cameron, A.D. and Ginsberg, N.A. and Lin, Y.-S. and Chen, M.; Yeang, Chen-Hsiang;Ma, Gwo-Chin;Shih, Jin-Chung;Yang, Yu-Shih;Chen, Chih-Ping;Chang, Shun-Ping;Wu, Sheng-Hai;Liu, Chin-San;Kuo, Shou-Jen;Chou, Hung-Chieh;Hwu, Wuh-Liang;Cameron, Alan D.;Ginsberg, Norman A.;Lin, Yi-Shing;Chen, Ming; 楊友仕 ;施景中 ;胡務亮 ;周弘傑 ;陳明; HUNG-CHIEH CHOU; Yeang, Chen-Hsiang; Ma, Gwo-Chin; MING CHEN; YU-SHIH YANG; Shih, Jin-Chung; JIN-CHUNG SHIH; Yang, Yu-Shih; WUH-LIANG HWU; Chen, Chih-Ping; Chang, Shun-Ping; Wu, Sheng-Hai; Liu, Chin-San; Kuo, Shou-Jen; Chou, Hung-Chieh; Hwu, Wuh-Liang; Cameron, Alan D.; Ginsberg, Norman A.; Lin, Yi-Shing; Chen, Ming
臺大學術典藏 2018-09-10T08:50:12Z Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation Chen, C.-P.;Su, Y.-N.;Chen, M.;Huang, J.-P.;Tsai, F.-J.;Wu, P.-C.;Chen, W.-L.;Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T08:50:12Z Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome Chen, C.-P. Chen, M. Ma, G.-C. Chang, S.-P. Chen, Y.-Y. Wu, P.-C. Chen, L.-F. Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T08:50:12Z Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4 Chen, W.-L.;Pan, C.-W.;Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Tsai, Fuu-Jen;Chern, Schu-Rern;Wu, Pei-Chen;Chen, Li-Feng;Wang, Wayseen; CHEN, CHIH-PING;CHEN, MING;SU, YI-NING;TSAI, FUU-JEN;CHERN, SCHU-RERN;WU, PEI-CHEN;CHEN, LI-FENG;WANG, WAYSEEN; 陳持平;陳明;蘇怡寧;蔡輔仁;陳樹人;吳佩臻;陳麗鳳;王偉信; MING CHEN; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; CHEN, LI-FENG; WANG, WAYSEEN
臺大學術典藏 2018-09-10T08:50:12Z Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature review Chen, Y.-T.;Wang, W.;Chen, Chih-Ping;Chen, Ming;Pan, Yi-Ju;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Wang, Wayseen; CHEN, CHIH-PING;CHEN, MING;PAN, YI-JU;SU, YI-NING;CHERN, SCHU-RERN;TSAI, FUU-JEN;WANG, WAYSEEN; 陳持平;陳明;潘怡如;蘇怡寧;陳樹人;蔡輔仁;王偉信; MING CHEN; CHEN, CHIH-PING; CHEN, MING; PAN, YI-JU; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WANG, WAYSEEN
臺大學術典藏 2018-09-10T08:50:11Z Aseptic necrosis of bilateral femoral heads after pregnancy Lin, Y.-C. Chen, W.-S. Chang, C.-C. Chen, M. Yu, C.-T.; MING CHEN
臺大學術典藏 2018-09-10T08:50:11Z Complex chromosome rearrangement 46,XY, der(9)t(Y;9)(q12;p23) in a girl with sex reversal and mental retardation Lee, I.-W.;Chou, Y.-Y.;Hsu, K.-F.;Chou, P.-Y.;Chen, M.;Kuo, P.-L.;Lin, S.-J.; MING CHEN
臺大學術典藏 2018-09-10T08:50:11Z Intrapartum uterine rupture associated with a scarred cervix because of a previous rupture of cystic cervical endometriosis Chen, Z.H.Y.;Chen, M.;Tsai, H.-D.;Wu, C.-H.; MING CHEN
臺大學術典藏 2018-09-10T08:50:11Z Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses Chen, C.-P. Lin, S.-P. Chen, M. Su, Y.-N. Chern, S.-R. Wang, T.-Y. Liu, Y.-P. Tsai, F.-J. Lee, C.-C. Chen, Y.-J. Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T08:50:10Z A 20.5-MB germline deletion of 13q13.1→q14.3 and somatic mutations of the RB1 gene in an 8-year-old girl with unilateral retinoblastoma, developmental delay and mental retardation Chen, C.-P.;Kao, L.-Y.;Su, Y.-N.;Chen, M.;Chang, S.-D.;Wang, W.; MING CHEN
臺大學術典藏 2018-09-10T08:22:12Z CK7+/CK20 - Merkel cell carcinoma presenting as inguinal subcutaneous nodules with subsequent epidermotropic metastasis Tsai, Y.-Y. and Hsiao, C.-H. and Chiu, H.-C. and Chen, M. and Tsai, T.-F.; HSIEN-CHING CHIU; MING CHEN; TSEN-FANG TSAI
臺大學術典藏 2018-09-10T07:47:27Z Ruptured Corpus Luteum with Hemoperitoneum: Case Characteristics and Demographic Changes Over Time Wang, Y.-F.;Ho, Wen-Kuang;Wu, Hsin-Hung;Tsai, Horng -Der;Chen, Tze-Ho;Chen, Ming; HO, WEN-KUANG;WU, HSIN-HUNG;TSAI, HORNG -DER;CHEN, TZE-HO;CHEN, MING; 何文光;吳信宏;蔡鴻德;陳子和;陳明; MING CHEN; HO, WEN-KUANG; WU, HSIN-HUNG; TSAI, HORNG -DER; CHEN, TZE-HO; CHEN, MING

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