| 臺大學術典藏 |
2020-02-14T02:50:05Z |
Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison
|
Hung C.-C.; Lee C.-N.; Lin C.-Y.; WEN-FANG CHENG; Chen C.-A.; Hsieh S.-T.; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Lin W.-L. |
| 臺大學術典藏 |
2020-02-13T05:52:20Z |
The F-box protein Fbxo7 interacts with human inhibitor of apoptosis protein cIAP1 and promotes cIAP1 ubiquitination
|
Chang Y.-F.;Cheng C.-M.;Chang L.-K.;Jong Y.-J.;Yuo C.-Y.; Chang Y.-F.; Cheng C.-M.; Chang L.-K.; Jong Y.-J.; Yuo C.-Y.; LI-KWAN CHANG |
| 臺大學術典藏 |
2020-02-12T04:06:27Z |
Quantification of relative gene dosage by single-base extension and high-performance liquid chromatography: Application to the SMN1/SMN2 gene
|
Su Y.-N.;Lin W.-L;Cheng W.-F;Chen C.-A;Jong Y.-J;Chen C.-P;CHIEN-NAN LEE;Hung C.-C; Hung C.-C; CHIEN-NAN LEE; Chen C.-P; Jong Y.-J; Chen C.-A; Cheng W.-F; Lin W.-L; Su Y.-N. |
| 臺大學術典藏 |
2020-02-12T04:06:11Z |
Molecular assay of -�\3.7 and -�\4.2 deletions causing �\-thalassemia by denaturing high-performance liquid chromatography
|
Hsu S.-M.;Su Y.-N;Lin W.-L;Hsieh W.-S;Jong Y.-J;Chen C.-P;CHIEN-NAN LEE;Hung C.-C; Hung C.-C; CHIEN-NAN LEE; Chen C.-P; Jong Y.-J; Hsieh W.-S; Lin W.-L; Su Y.-N; Hsu S.-M. |
| 臺大學術典藏 |
2020-02-12T04:06:10Z |
Use of multiplex PCR and CE for gene dosage quantification and its biomedical application for SMN, PMP22, and �\-globin genes
|
Su Y.-N.;CHIEN-NAN LEE;Lin W.-L;Liu M.S;Hsieh W.-S;Hsieh S.-T;Jong Y.-J;Chang Y.-F;Chang C.-H;Lin C.-Y;Chien S.-C;Hung C.-C; Hung C.-C; Chien S.-C; Lin C.-Y; Chang C.-H; Chang Y.-F; Jong Y.-J; Hsieh S.-T; Hsieh W.-S; Liu M.S; Lin W.-L; CHIEN-NAN LEE; Su Y.-N. |
| 臺大學術典藏 |
2020-02-12T04:06:08Z |
Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis
|
Lin W.-L.;Su Y.-N;Hsieh W.-S;Chen C.-P;Jong Y.-J;Chang C.-H;CHIEN-NAN LEE;Hung C.-C; Hung C.-C; CHIEN-NAN LEE; Chang C.-H; Jong Y.-J; Chen C.-P; Hsieh W.-S; Su Y.-N; Lin W.-L. |
| 臺大學術典藏 |
2020-02-12T04:06:08Z |
Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison
|
Lin W.-L.;Su Y.-N;Jong Y.-J;Yang C.-C;Hsieh S.-T;Chen C.-A;Cheng W.-F;Lin C.-Y;CHIEN-NAN LEE;Hung C.-C; Hung C.-C; CHIEN-NAN LEE; Lin C.-Y; Cheng W.-F; Chen C.-A; Hsieh S.-T; Yang C.-C; Jong Y.-J; Su Y.-N; Lin W.-L. |
| 臺大學術典藏 |
2020-02-06T05:22:29Z |
Quantification of relative gene dosage by single-base extension and high-performance liquid chromatography: Application to the SMN1/SMN2 gene
|
Jong Y.-J.; Chen C.-P.; Lee C.-N.; Su Y.-N.; Hung C.-C.; WEN-FANG CHENG; Lin W.-L.; Jong Y.-J.; Chen C.-A.; Chen C.-P.; Lee C.-N.; Hung C.-C.; Su Y.-N.;Lin W.-L.;WEN-FANG CHENG;Chen C.-A.;Jong Y.-J.;Chen C.-P.;Lee C.-N.;Hung C.-C.; Chen C.-A.; WEN-FANG CHENG; Lin W.-L.; Su Y.-N. |
| 臺大學術典藏 |
2020-02-06T05:22:22Z |
Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison
|
Lin W.-L.;Su Y.-N.;Jong Y.-J.;Yang C.-C.;Hsieh S.-T.;Chen C.-A.;WEN-FANG CHENG;Lin C.-Y.;Lee C.-N.;Hung C.-C.; Hung C.-C.; Lee C.-N.; Lin C.-Y.; WEN-FANG CHENG; Chen C.-A.; Hsieh S.-T.; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Lin W.-L.; Hung C.-C.; Lee C.-N.; Lin C.-Y.; WEN-FANG CHENG; Chen C.-A.; Hsieh S.-T.; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Lin W.-L. |
| 臺大學術典藏 |
2020-02-03T08:15:21Z |
Multiplex ligation-dependent probe amplification identification of deletions and duplications of the duchenne muscular dystrophy gene in Taiwanese subjects
|
Hsiao-Lin Hwa;Chang Y.-Y.;Chen C.-H.;Kao Y.-S.;Jong Y.-J.;Chao M.-C.;Ko T.-M.; HSIAO-LIN HWA; Chang Y.-Y.; Chen C.-H.; Kao Y.-S.; Jong Y.-J.; Chao M.-C.; Ko T.-M. |
| 臺大學術典藏 |
2020-02-03T08:15:20Z |
Small mutations of the DMD gene in Taiwanese families
|
HSIAO-LIN HWA; Chang Y.-Y.; Huang C.-H.; Chen C.-H.; Kao Y.-S.; Jong Y.-J.; Chao M.-C.; Ko T.-M. |
| 臺大學術典藏 |
2020-01-22T07:50:49Z |
Quantification of relative gene dosage by single-base extension and high-performance liquid chromatography: Application to the SMN1/SMN2 gene
|
Hung C.-C.;Lee C.-N.;Chen C.-P.;Jong Y.-J.;Chi-An Chen;Cheng W.-F.;Lin W.-L.;Su Y.-N.; Hung C.-C.; Lee C.-N.; Chen C.-P.; Jong Y.-J.; CHI-AN CHEN; Cheng W.-F.; Lin W.-L.; Su Y.-N. |
| 國立成功大學 |
2020 |
Segmental isodisomy in Prader–Willi syndrome patients: The experience of a single diagnostic center
|
Pan, Y.-W.;Chang, Chang C.-W.;Jong, Y.-J.;Chou, Y.-Y.;Kuo, P.-L. |
| 臺大學術典藏 |
2018-09-10T07:13:27Z |
Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis
|
Hung, C.-C.;Lee, C.-N.;Chang, C.-H.;Jong, Y.-J.;Chen, C.-P.;Hsieh, W.-S.;Su, Y.-N.;Lin, W.-L.; WU-SHIUN HSIEH; CHIEN-NAN LEE |
| 臺大學術典藏 |
2018-09-10T06:41:37Z |
Use of multiplex PCR and CE for gene dosage quantification and its biomedical application for SMN, PMP22, and α-globin genes
|
Hung, C.-C.;Chien, S.-C.;Lin, C.-Y.;Chang, C.-H.;Chang, Y.-F.;Jong, Y.-J.;Hsieh, S.-T.;Hsieh, W.-S.;Liu, M.S.;Lin, W.-L.;Lee, C.-N.;Su, Y.-N.; WU-SHIUN HSIEH; SUNG-TSANG HSIEH; CHIEN-NAN LEE |
| 臺大學術典藏 |
2018-09-10T06:41:36Z |
Molecular assay of -α3.7and -α4.2deletions causing α-thalassemia by denaturing high-performance liquid chromatography
|
Hung, C.-C.;Lee, C.-N.;Chen, C.-P.;Jong, Y.-J.;Hsieh, W.-S.;Lin, W.-L.;Su, Y.-N.;Hsu, S.-M.; WU-SHIUN HSIEH; CHIEN-NAN LEE |
| 臺大學術典藏 |
2016 |
Increased risks of tic disorders in children with epilepsy: A nation-wide population-based case-control study in Taiwan
|
Weng W.-C.; Huang H.-L.; Wong L.C.; Jong Y.-J.; Yin Y.-J.; Chen H.-A.; WANG-TSO LEE; Ho S.-Y. |
| 國立交通大學 |
2014-12-08T15:32:21Z |
Benign reversible course in infants manifesting clinicopathological features of fatal mitochondrial myopathy due to m.14674 T > C mt-tRNA(Glu) mutation
|
Chen, T. -H.; Tu, Y. -F.; Goto, Y. -I.; Jong, Y. -J. |
| 臺大學術典藏 |
2014 |
Development of a feasible assay for the detection of GAA mutations in patients with Pompe disease
|
Er T.-K.; Chen C.-C.; YIN-HSIU CHIEN; Liang W.-C.; Kan T.-M.; Jong Y.-J. |
| 臺大學術典藏 |
2011 |
Computational analysis of a novel mutation in ETFDH gene highlights its long-range effects on the FAD-binding motif
|
Er T.-K.; Chen C.-C.; Liu Y.-Y.; Chang H.-C.; YIN-HSIU CHIEN; Chang J.-G.; Hwang J.-K.; Jong Y.-J. |
| 臺大學術典藏 |
2008 |
Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison
|
Lee C.-N.; Lin C.-Y.; Cheng W.-F.; CHI-AN CHEN; Hsieh S.-T.; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Lin W.-L.; Hung C.-C. |
| 臺大學術典藏 |
2007 |
Molecular assay of -α3.7 and -α4.2 deletions causing α-thalassemia by denaturing high-performance liquid chromatography
|
Hung C.-C.;Lee C.-N.;Chen C.-P.;Jong Y.-J.;Hsieh W.-S.;Win-Li Lin;Su Y.-N.;Hsu S.-M.; Hung C.-C.; Lee C.-N.; Chen C.-P.; Jong Y.-J.; Hsieh W.-S.; Win-Li Lin; Su Y.-N.; Hsu S.-M. |
| 國立臺灣大學 |
2004 |
Analysis of chromosome abnormalities by comparative genomic hybridization in malignant peripheral primitive neuroectodermal tumor of the ovary
|
Chow, S-N; Lin, M-C; Shen, J; Wang, S; Jong, Y-J; Chien, C-H |
| 國立彰化師範大學 |
2000-01 |
A Mouse Model for Spinal Muscular Atrophy
|
Hsieh-Li, H. M. ; Chang, J. G. ; Jong, Y. J. ; Wu, M. H. ; Wang, Nancy M. ; Tsai, C. H. ; Li, H. |
| 國立臺灣大學 |
1994 |
Guillain-Barre Syndrome in Children:A Cooperative Study in Taiwan
|
洪焜隆; Wang, H. S.; Liou, W. Y.; Mak, S. C.; Chi, C. S.; Shen, E. Y.; Lin, M. I.; 王本榮; Shen, Y. Z.; Chang, K. P.; Ko, F. J.; Jong, Y. J.; Chiang, C. H.; Chen, Y. J.; 何美美; 洪焜隆; Wang, H. S.; Liou, W. Y.; Mak, S. C.; Chi, C. S.; Shen, E. Y.; Lin, M. I.; 王本榮; Shen, Y. Z.; Chang, K. P.; Ko, F. J.; Jong, Y. J.; Chiang, C. H.; Chen, Y. J.; Ho, Mei-Mei |
