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Showing items 26-50 of 140 (6 Page(s) Totally) << < 1 2 3 4 5 6 > >> View [10|25|50] records per page
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
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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
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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
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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
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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)
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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
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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.
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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
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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
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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
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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
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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
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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
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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
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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?
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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.
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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
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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
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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
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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
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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
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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
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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
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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
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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
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Chen, C.-P. Chen, M. Ma, G.-C. Chang, S.-P. Chen, Y.-Y. Wu, P.-C. Chen, L.-F. Wang, W.; MING CHEN |
Showing items 26-50 of 140 (6 Page(s) Totally) << < 1 2 3 4 5 6 > >> View [10|25|50] records per page
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