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"ke y y"的相关文件
显示项目 31-44 / 44 (共2页)
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| 臺大學術典藏 |
2018-09-10T14:57:46Z |
Learning user reformulation behavior for query auto-completion
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Jiang, J.-Y.;Ke, Y.-Y.;Chien, P.-Y.;Cheng, P.-J.; Jiang, J.-Y.; Ke, Y.-Y.; Chien, P.-Y.; Cheng, P.-J.; PU-JEN CHENG |
| 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
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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.;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
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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 |
2018-09-10T07:13:32Z |
Phenotype and Genotype of Two Taiwanese Cystic Fibrosis Siblings and a Survey of Delta F508 in East Asians
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Lin, C.-J.;Chang, S.-P.;Ke, Y.-Y.;Chiu, H.-Y.;Tsao, L.-Y.;Chen, M.; 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
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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 |
| 臺大學術典藏 |
2018-09-10T06:41:41Z |
Interstitial deletion 13q31 associated with normal phenotype: Cytogenetic study of a family with concomitant segregation of reciprocal translocation and interstitial deletion
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Ke, Y.-Y.;Lee, D.-J.;Ma, G.-C.;Lee, M.-H.;Wang, B.-T.;Chen, M.; MING CHEN |
| 臺大學術典藏 |
2018-09-10T04:07:45Z |
Photoluminescence study of hydrogen passivation in InAs1-xN x/InGaAs single-quantum well on InP
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Ke, Y.Y.;Ya, M.H.;Chen, Y.F.;Wang, J.S.;Lin, H.H.; Ke, Y.Y.; Ya, M.H.; Chen, Y.F.; Wang, J.S.; Lin, H.H.; HAO-HSIUNG LIN; YANG-FANG CHEN |
| 臺大學術典藏 |
2018 |
Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan
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Tsao P.-N.; Ke Y.-Y.; Lin Y.-H.; Lin Y.-H.; Hung C.-C.; Su Y.-N.; Hsu W.-C.; Hsieh W.-S.; Huang L.-M.; Chen-Chi Wu; Hsu C.-J.; Lu C.-Y. |
| 臺大學術典藏 |
2018 |
Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan
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Hsu W.-C.; Su Y.-N.; Hung C.-C.; Lin Y.-H.; Lin Y.-H.; Ke Y.-Y.; PO-NIEN TSAO; Lu C.-Y.; Lu C.-Y.;Po-Nien Tsao;Ke Y.-Y.;Lin Y.-H.;Lin Y.-H.;Hung C.-C.;Su Y.-N.;Hsu W.-C.;Hsieh W.-S.;Huang L.-M.;Wu C.-C.;Hsu C.-J.; Hsieh W.-S.; Huang L.-M.; Wu C.-C.; Hsu C.-J. |
| 臺大學術典藏 |
2016 |
Long-term galsulfase enzyme replacement therapy in Taiwanese mucopolysaccharidosis VI patients: A case series
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Lin H.-Y.; Chuang C.-K.; Wang C.-H.; YIN-HSIU CHIEN; Wang Y.-M.; Tsai F.-J.; Chou Y.-Y.; Lin S.J.; Pan H.-P.; Niu D.-M.; Hwu W.-L.; Ke Y.-Y.; Lin S.-P. |
| 臺大學術典藏 |
2013 |
Erratum: Enzyme replacement therapy for mucopolysaccharidosis VI - Experience in Taiwan (Journal of Inherited Metabolic Disease DOI: 10.1007/s20545-101-9212-5)
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Lin H.-Y.; Chen M.-R.; Chuang C.-K.; Chen C.-P.; Lin D.-S.; Chien Y.-H.; Ke Y.-Y.; Tsai F.-J.; Pan H.-P.; Lin S.-J.; Hwu W.-L.; Niu D.-M.; NI-CHUNG LEE; Lin S.-P. |
| 臺大學術典藏 |
2013 |
erratum: Enzyme replacement therapy for mucopolysaccharidosis VI - Experience in Taiwan (Journal of Inherited Metabolic Disease DOI: 10.1007/s20545-101-9212-5)
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Lin H.-Y.; Chen M.-R.; Chuang C.-K.; Chen C.-P.; Lin D.-S.; YIN-HSIU CHIEN; Ke Y.-Y.; Tsai F.-J.; Pan H.-P.; Lin S.-J.; Hwu W.-L.; Niu D.-M.; Lee N.-C.; Lin S.-P. |
| 臺大學術典藏 |
2011 |
Inhibition of HIV-1 Tat-mediated transcription by a coumarin derivative, BPRHIV001, through the Akt pathway
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Lin P.-H. ;Ke Y.-Y. ;Su C.-T. ;Shiao H.-Y. ;Hsieh H.-P. ;Chao Y.-K. ;Lee C.-N. ;Chuan-Liang Kao ;Chao Y.-S. ;Chang S.-Y.; Lin P.-H.; Ke Y.-Y.; Su C.-T.; Shiao H.-Y.; Hsieh H.-P.; Chao Y.-K.; Lee C.-N.; CHUAN-LIANG KAO; Chao Y.-S.; Chang S.-Y. |
| 國立臺灣大學 |
2002 |
Photoluminescence study of hydrogen passivation in InAs[sub 1-x]N[sub x]/InGaAs single-quantum well on InP
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Ke, Y. Y.; Ya, M. H.; Chen, Y. F.; Wang, J. S.; Lin, H. H. |
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