| 臺大學術典藏 |
2022-09-15T05:47:47Z |
Preimplantation genetic diagnosis in hereditary hearing impairment
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Chen H.-L.; Lin P.-H.; Chiang Y.-T.; Huang W.-J.; Lin C.-F.; Ma G.-C.; Chang S.-P.; Fan J.-Y.; Lin S.-Y.; Chen-Chi Wu; Chen M. |
| 臺大學術典藏 |
2021-05-25T06:35:56Z |
The spectrum of the factor 8 (F8) defects in Taiwanese patients with haemophilia A
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Ma G.-C.; Chang S.-P.; Chen M.; Kuo S.-J.; Chang C.-S.; MING-CHING SHEN |
| 臺大學術典藏 |
2021-05-25T06:35:53Z |
De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD
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MING-CHING SHEN; Chen M.; Ma G.-C.; Chang S.-P.; Lin C.-Y.; Lin B.-D.; Hsieh H.-N. |
| 臺大學術典藏 |
2021-05-25T06:35:53Z |
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.; MING-CHING SHEN |
| 臺大學術典藏 |
2021-05-25T06:35:52Z |
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-CHING SHEN; Wu W.-J.; Cheng P.-J.; Ma G.-C.; Li W.-C.; Liou J.-D.; Chang C.-S.; Lin W.-H.; Chen M. |
| 臺大學術典藏 |
2021-02-04T06:46:45Z |
Proinflammatory macrophage migratory inhibition factor and interleukin-6 are concentrated in pleural effusion of human fetuses with prenatal chylothorax
|
Chen M.;Hsieh C.-Y.;Jin-Chung Shih;Chou C.-H.;Ma G.-C.;Chen T.-H.;Lee T.-H.;Tsai H.-D.;Cameron A.D.;Chen C.-P.; Chen M.; Hsieh C.-Y.; JIN-CHUNG SHIH; Chou C.-H.; Ma G.-C.; Chen T.-H.; Lee T.-H.; Tsai H.-D.; Cameron A.D.; Chen C.-P. |
| 臺大學術典藏 |
2021-02-04T06:46:42Z |
Genetic evaluation and management of fetal chylothorax: Review and insights from a case of Noonan syndrome
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Chen C.-H.;Chen T.-H.;Kuo S.-J.;Chen C.-P.;Lee D.-J.;Ke Y.-Y.;Yeh K.-T.;Ma G.-C.;Liu C.-S.;Jin-Chung Shih;Chen M.; Chen C.-H.; Chen T.-H.; Kuo S.-J.; Chen C.-P.; Lee D.-J.; Ke Y.-Y.; Yeh K.-T.; Ma G.-C.; Liu C.-S.; JIN-CHUNG SHIH; Chen M. |
| 臺大學術典藏 |
2021-02-04T06:04:29Z |
Application of molecular cytogenetic techniques to characterize the aberrant Y chromosome arising de novo in a male fetus with mosaic 45,X and solve the discrepancy between karyotyping, chromosome microarray, and multiplex ligation dependent probe amplification
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Lin S.-Y.;Chien-Nan Lee;Peng A.-Y.;Yuan T.-J.;Lee D.-J.;Lin W.-H.;Ma G.-C.;Chen M.; Lin S.-Y.; CHIEN-NAN LEE; Peng A.-Y.; Yuan T.-J.; Lee D.-J.; Lin W.-H.; Ma G.-C.; Chen M. |
| 臺大學術典藏 |
2020-12-28T08:14:24Z |
Genome-wide normalized score: A novel algorithm to detect fetal trisomy 21 during non-invasive prenatal testing
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Chen M.; Yeang C.H.; Ma G.C.; Hsu H.W.; Lin Y.S.; Chang S.M.; Cheng P.J.; Chen C.A.; YEN-HSUAN NI |
| 臺大學術典藏 |
2020-12-28T08:14:21Z |
Validating a rapid, real-time, PCR-based direct mutation detection assay for preimplantation genetic diagnosis
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Lee Y.-C.; Lin W.-H.; Wu S.-H.; Chang S.-P.; Chen H.-F.; YEN-HSUAN NI; Chen C.-A.; Ma G.-C.; Ginsberg N.A.; You E.-M.; Tsai F.-P.; Chen M. |
| 臺大學術典藏 |
2020-12-24T06:16:57Z |
Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints
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Ke Y.-Y.; Wang T.-J.; Lee D.-J.; Ma G.-C.; Lee N.-C.; Chen M.; YIN-HSIU CHIEN; Hwu W.-L. |
| 臺大學術典藏 |
2020-12-16T02:25:44Z |
Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints
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Lee N.-C.;Chen M.;Ma G.-C.;Lee D.-J.;Wang T.-J.;Ke Y.-Y.;Chien Y.-H.;Wuh-Liang Hwu; Lee N.-C.; Chen M.; Ma G.-C.; Lee D.-J.; Wang T.-J.; Ke Y.-Y.; Chien Y.-H.; WUH-LIANG HWU |
| 臺大學術典藏 |
2020-12-16T02:25:39Z |
Experimental treatment of bilateral fetal chylothorax using in-utero pleurodesis
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Yang Y.-S.; Ma G.-C.; Shih J.-C.; Chen C.-P.; Chou C.-H.; Yeh K.-T.; Kuo S.-J.; Chen T.-H.; WUH-LIANG HWU; Lee T.-H.; Chen M. |
| 臺大學術典藏 |
2020-12-16T02:25:39Z |
Preimplantation and prenatal genetic diagnosis of aromatic L-amino aciddecarboxylase deficiency with an amplification refractory mutation system-quantitative polymerase chain reaction
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Kuo S.-J.;Ma G.-C.;Chang S.-P.;Wu H.-H.;Chen C.-P.;Chang T.-M.;Lin W.-H.;Wu S.-H.;Lee M.-H.;Wuh-Liang Hwu;Chen M.; Kuo S.-J.; Ma G.-C.; Chang S.-P.; Wu H.-H.; Chen C.-P.; Chang T.-M.; Lin W.-H.; Wu S.-H.; Lee M.-H.; WUH-LIANG HWU; Chen M. |
| 臺大學術典藏 |
2020-12-16T02:25:37Z |
Genome-wide gene expression analysis implicates the immune response and lymphangiogenesis in the pathogenesis of fetal chylothorax
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Yeang C.-H.; Ma G.-C.; Shih J.-C.; Yang Y.-S.; Chen C.-P.; Chang S.-P.; Wu S.-H.; Liu C.-S.; Kuo S.-J.; Chou H.-C.; WUH-LIANG HWU; Cameron A.D.; Ginsberg N.A.; Lin Y.-S.; Chen M. |
| 臺大學術典藏 |
2020-12-09T01:38:34Z |
Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints
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Ni-Chung Lee;Chen M.;Ma G.-C.;Lee D.-J.;Wang T.-J.;Ke Y.-Y.;Chien Y.-H.;Hwu W.-L.; NI-CHUNG LEE; Chen M.; Ma G.-C.; Lee D.-J.; Wang T.-J.; Ke Y.-Y.; Chien Y.-H.; Hwu W.-L. |
| 臺大學術典藏 |
2020-11-27T08:14:26Z |
Proinflammatory macrophage migratory inhibition factor and interleukin-6 are concentrated in pleural effusion of human fetuses with prenatal chylothorax
|
Chen M.;Chang-Yao Hsieh;Shih J.-C.;Chou C.-H.;Ma G.-C.;Chen T.-H.;Lee T.-H.;Tsai H.-D.;Cameron A.D.;Chen C.-P.; Chen M.; CHANG-YAO HSIEH; Shih J.-C.; Chou C.-H.; Ma G.-C.; Chen T.-H.; Lee T.-H.; Tsai H.-D.; Cameron A.D.; Chen C.-P. |
| 臺大學術典藏 |
2020-03-03T02:33:33Z |
Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonography
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Ma G.-C.; Chang S.-D.; Chang Y.; Chang S.-P.; Yang C.-W.; MING-JEN LEE; Lee T.-H.; Chen M. |
| 臺大學術典藏 |
2020-03-02T08:11:04Z |
Preimplantation genetic diagnosis and screening: Current status and future challenges
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Chen H.-F.; Chen S.-U.; Ma G.-C.; SUNG-TSANG HSIEH; Tsai H.-D.; Yang Y.-S.; Chen M. |
| 臺大學術典藏 |
2020-03-02T08:11:01Z |
Preimplantation genetic diagnosis of neurodegenerative diseases: Review of methodologies and report of our experience as a regional reference laboratory
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Liao C.-H.;Chang M.-Y.;Ma G.-C.;Chang S.-P.;Lin C.-F.;Lin W.-H.;Chen H.-F.;Chen S.-U.;Lee Y.-C.;Chao C.-C.;Chen M.;Sung-Tsang Hsieh; Liao C.-H.; Chang M.-Y.; Ma G.-C.; Chang S.-P.; Lin C.-F.; Lin W.-H.; Chen H.-F.; Chen S.-U.; Lee Y.-C.; Chao C.-C.; Chen M.; SUNG-TSANG HSIEH |
| 臺大學術典藏 |
2020-03-02T03:10:52Z |
Detection of 22q11.2 microduplication by cell-free DNA screening and chromosomal microarray in fetus with multiple anomalies
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Wu W.-J.; Ma G.-C.; Lin Y.-S.; Yeang C.-H.; Ni Y.-H.; Li W.-C.; Tsai H.-D.; SUSAN SHUR-FEN GAU; Chen M. |
| 臺大學術典藏 |
2020-02-17T08:07:05Z |
Experimental treatment of bilateral fetal chylothorax using in-utero pleurodesis
|
YU-SHIH YANG; Ma G.-C; Shih J.-C; Chen C.-P; Chou C.-H; Yeh K.-T; Kuo S.-J; Chen T.-H; Hwu W.-L; Lee T.-H; Chen M. |
| 臺大學術典藏 |
2020-02-17T08:07:04Z |
Genome-wide gene expression analysis implicates the immune response and lymphangiogenesis in the pathogenesis of fetal chylothorax
|
Yeang C.-H; Ma G.-C; Shih J.-C; YU-SHIH YANG; Chen C.-P; Chang S.-P; Wu S.-H; Liu C.-S; Kuo S.-J; Chou H.-C; Hwu W.-L; Cameron A.D; Ginsberg N.A; Lin Y.-S; Chen M. |
| 臺大學術典藏 |
2020-02-17T08:07:02Z |
Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization
|
Ma G.-C.; Chen M; YU-SHIH YANG; Shih J.-C; Lee M.-L; Chen C.-A; Cameron A.D; Ginsberg N.A; Chou C.-H; Lin Y.-S; Lee D.-J; Lin W.-H |
| 臺大學術典藏 |
2020-02-17T08:07:02Z |
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; YU-SHIH YANG; Shih J.-C; Lin W.-H; Lee D.-J; Lin Y.-S; Chou C.-H; Cameron A.D; Ginsberg N.A; Chen C.-A; Lee M.-L; Ma G.-C. |
