| 臺大學術典藏 |
2022-09-15T05:47:47Z |
Preimplantation genetic diagnosis in hereditary hearing impairment
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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. |
| 臺大學術典藏 |
2020-02-17T08:07:00Z |
Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: Validation and verification
|
YU-SHIH YANG; Chang S.-P; Chen H.-F; Ma G.-C; Lin W.-H; Lin C.-F; Tsai F.-P; Wu C.-H; Tsai H.-D; Lee T.-H; Chen M. |
| 臺大學術典藏 |
2020-02-17T08:06:59Z |
A pilot proof-of-principle study to compare fresh and vitrified cycle preimplantation genetic screening by chromosome microarray and next generation sequencing
|
Chen M.; Chiu C; Lin C.-F; Tsai F.-P; Lin W.-H; Ma G.-C; Chen H.-F; YU-SHIH YANG |
| 臺大學術典藏 |
2020-02-17T08:06:59Z |
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; YU-SHIH YANG; Lin W.-H; Tsai F.-P; Lin C.-F; Chiu C; Chen M. |
| 臺大學術典藏 |
2020-02-17T08:06:57Z |
Preimplantation genetic diagnosis and screening: Current status and future challenges
|
Chen S.-U; Chen H.-F; Chen H.-F;Chen S.-U;Ma G.-C;Hsieh S.-T;Tsai H.-D;Yu-Shih Yang;Chen M.; Ma G.-C; Hsieh S.-T; Tsai H.-D; YU-SHIH YANG; Chen M. |
| 臺大學術典藏 |
2020-02-17T08:06:57Z |
Preimplantation genetic diagnosis and screening: Current status and future challenges
|
Chen H.-F;Chen S.-U;Ma G.-C;Hsieh S.-T;Tsai H.-D;Yu-Shih Yang;Chen M.; Chen H.-F; Chen S.-U; Ma G.-C; Hsieh S.-T; Tsai H.-D; YU-SHIH YANG; Chen M. |
| 臺大學術典藏 |
2020-02-12T04:05:37Z |
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
|
Chen M.;Ma G.-C;Lin W.-H;Lee D.-J;Yuan T.-J;Peng A.-Y;CHIEN-NAN LEE;Lin S.-Y; 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 |
2020-02-10T06:49:07Z |
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
|
Shin-Yu Lin;Lee C.-N;Peng A.-Y;Yuan T.-J;Lee D.-J;Lin W.-H;Ma G.-C;Chen M.; SHIN-YU LIN; Lee C.-N; Peng A.-Y; Yuan T.-J; Lee D.-J; Lin W.-H; Ma G.-C; Chen M. |
| 臺大學術典藏 |
2020-02-06T06:49:52Z |
Preimplantation genetic diagnosis and screening: Current status and future challenges
|
Chen H.-F;Shee-Uan Chen;Ma G.-C;Hsieh S.-T;Tsai H.-D;Yang Y.-S;Chen M.; Chen H.-F; SHEE-UAN CHEN; Ma G.-C; Hsieh S.-T; Tsai H.-D; Yang Y.-S; Chen M. |
| 臺大學術典藏 |
2020-02-06T06:49:51Z |
Preimplantation genetic diagnosis of neurodegenerative diseases: Review of methodologies and report of our experience as a regional reference laboratory
|
Liao C.-H;Chang M.-Y;Ma G.-C;Chang S.-P;Lin C.-F;Lin W.-H;Chen H.-F;Shee-Uan Chen;Lee Y.-C;Chao C.-C;Chen M;Hsieh S.-T.; Liao C.-H; Chang M.-Y; Ma G.-C; Chang S.-P; Lin C.-F; Lin W.-H; Chen H.-F; SHEE-UAN CHEN; Lee Y.-C; Chao C.-C; Chen M; Hsieh S.-T. |
| 臺大學術典藏 |
2020-01-22T07:50:33Z |
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.;Yang Y.-S.;Shih J.-C.;Lin W.-H.;Lee D.-J.;Lin Y.-S.;Chou C.-H.;Cameron A.D.;Ginsberg N.A.;Chi-An Chen;Lee M.-L.;Ma G.-C.; Chen M.; Yang Y.-S.; Shih J.-C.; Lin W.-H.; Lee D.-J.; Lin Y.-S.; Chou C.-H.; Cameron A.D.; Ginsberg N.A.; CHI-AN CHEN; Lee M.-L.; Ma G.-C. |
| 臺大學術典藏 |
2020-01-22T07:50:32Z |
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.;Chi-An Chen;Ni Y.H.;Chen M.; Yeang C.H.; Ma G.C.; Hsu H.W.; Lin Y.S.; Chang S.M.; Cheng P.J.; CHI-AN CHEN; Ni Y.H.; Chen M. |
| 臺大學術典藏 |
2020-01-22T07:50:30Z |
Validating a rapid, real-time, PCR-based direct mutation detection assay for preimplantation genetic diagnosis
|
Chen H.-F.;Chang S.-P.;Wu S.-H.;Lin W.-H.;Lee Y.-C.;Ni Y.-H.;Chi-An Chen;Ma G.-C.;Ginsberg N.A.;You E.-M.;Tsai F.-P.;Chen M.; Chen H.-F.; Chang S.-P.; Wu S.-H.; Lin W.-H.; Lee Y.-C.; Ni Y.-H.; CHI-AN CHEN; Ma G.-C.; Ginsberg N.A.; You E.-M.; Tsai F.-P.; Chen M. |
| 臺大學術典藏 |
2019 |
Preimplantation genetic diagnosis of neurodegenerative diseases: Review of methodologies and report of our experience as a regional reference laboratory
|
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.;Chi-Chao Chao;Chen M.;Hsieh S.-T.; 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.; CHI-CHAO CHAO; Chen M.; Hsieh S.-T. |
| 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 |
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 |
2018-09-10T15:02:34Z |
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 |
2018-09-10T09:27:20Z |
Use of a cytogenetic whole-genome comparison to resolve phylogenetic relationships among three species: Implications for mammalian systematics and conservation biology
|
Ma, G.-C.; Lee, D.-J.; Chin, S.-C.; Chen, T.-L.; Tsao, H.-S.; Lin, W.-H.; Wu, S.-H.; Lin, C.-C.; Chen, M.; Yu, Hon-Tsen; Ma, Gwo-Chin; Lee, Dong-Jay; Chin, Shih-Chien; Chen, Ting-Li; Tsao, Hsien-Shao; Lin, Wen-Hsiang; Wu, Sheng-Hai; Lin, Chyi-Chyang; Chen, Ming; Yu, H.-T.; MING CHENet al.; Yu, Hon-Tsen; Chen, Chi-An |
| 臺大學術典藏 |
2018-09-10T08:50:11Z |
Molecular delineation of the Y-borne Sry gene in the Formosan pangolin (Manis pentadactyla pentadactyla) and its phylogenetic implications for Pholidota in extant mammals
|
Ma, G.-C.; Lee, D.-J.; Chin, S.-C.; Tsao, H.-S.; Wu, S.-H.; Shih, S.-Y.; Chen, M.Yu, Hon-Tsen; Ma, Gwo-Chin; Lee, Dong-Jay; Chin, Shih-Chien; Tsao, Hsien-Shao; Wu, Sheng-Hai; Shih, Shu-Yi; Chen, Ming; Yu, H.-T.; MING CHENet al.; Yu, Hon-Tsen; Ma, Gwo-Chin; Lee, Dong-Jay; Chin, Shih-Chien; Tsao, Hsien-Shao; Wu, Sheng-Hai; Shih, Shu-Yi; Chen, Ming |
| 臺大學術典藏 |
2018-09-10T07:47:26Z |
Differential Expression of NUDT9 at Different Phases of The Menstrual Cycle and in Different Components of Normal and Neoplastic Human Endometrium
|
Chen, L.-Y.;Chen, T.-H.;Wen, P.-Y.;Chou, C.-H.;Ying, T.-H.;Chang, S.-P.;Ma, G.-C.;Chen, M.Chen, Ling-Yun;Chen, Tze-Ho;Wen, Pao- Ying;Chou, Chia-Hung;Ying, Tsung-Ho;Chang, Shun-Ping;Ma, Gwo-Chin;Chen, Ming陳凌雲;陳子和;溫保英;周佳宏;應宗和;張舜評;馬國欽;陳明; CHEN, LING-YUN;CHEN, TZE-HO;WEN, PAO- YING;CHOU, CHIA-HUNG;YING, TSUNG-HO;CHANG, SHUN-PING;MA, GWO-CHIN;CHEN, MING; 陳凌雲;陳子和;溫保英;周佳宏;應宗和;張舜評;馬國欽;陳明; MING CHEN; CHEN, LING-YUN; CHEN, TZE-HO; WEN, PAO- YING; CHOU, CHIA-HUNG; YING, TSUNG-HO; CHANG, SHUN-PING; MA, GWO-CHIN; CHEN, MING |
| 臺大學術典藏 |
2018-09-10T07:47:26Z |
Genetic evaluation and management of fetal chylothorax: Review and insights from a case of Noonan syndrome
|
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.;Shih, J.-C.;Chen, M.; MING CHEN |
| 臺大學術典藏 |
2018-09-10T07:47:25Z |
A case of restrictive dermopathy with complete chorioamniotic membrane separation caused by a novel homozygous nonsense mutation in the ZMPST E24 gene
|
Chen, M.;Kuo, H.-H.;Huang, Y.-C.;Ke, Y.-Y.;Chang, S.-P.;Chen, C.-P.;Lee, D.-J.;Lee, M.-L.;Lee, M.-H.;Chen, T.-H.;Chen, C.-H.;Lin, H.-M.;Liu, C.-S.;Ma, G.-C.; MING CHEN |
| 臺大學術典藏 |
2018-09-10T07:13:33Z |
The spectrum of the factor 8 (F8) defects in Taiwanese patients with haemophilia A
|
Ma, G.-C.;Chang, S.-P.;Chen, M.;Kuo, S.-J.;Chang, C.-S.;Shen, M.-C.; MING CHEN |
| 臺大學術典藏 |
2018-09-10T07:02:24Z |
A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: Possible correlation with poor response to fetal therapy
|
Ma, G.-C.;Liu, C.-S.;Chang, S.-P.;Yeh, K.-T.;Ke, Y.-Y.;Chen, T.-H.;Wang, B.B.-T.;Kuo, S.-J.;Shih, J.-C.;Chen, M.; MING CHEN; JIN-CHUNG SHIH |
