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"pei lung chen"的相關文件
顯示項目 141-150 / 156 (共16頁)
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| 臺大學術典藏 |
2018-09-10T15:17:42Z |
Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome
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PEI-LUNG CHEN; Li, Huei-Ying; Ho, Hong-Nerng; Yang, Yu-Shih; Chen, Pei-Lung; Chen, M.-J. and Wei, S.-Y. and Yang, W.-S. and Wu, T.-T. and Li, H.-Y. and Ho, H.-N. and Yang, Y.-S. and Chen, P.-L.; 周妍君; Chen, Mei-Jou;Wei, Shin-Yi;Yang, Wei-Shiung;Wu, Tsai-Tzu;Li, Huei-Ying;Ho, Hong-Nerng;Yang, Yu-Shih;Chen, Pei-Lung; 楊友仕;陳美州;楊偉勛;何弘能;陳沛隆; 楊友仕;陳美州;楊偉勛;何弘能;陳沛隆; Chou, Yen-Chun; YU-SHIH YANG; Chen, Mei-Jou; Chou, Yen-Chun; HONG-NERNG HO; Wei, Shin-Yi; MEI-JOU CHEN; Yang, Wei-Shiung; Wu, Tsai-Tzu; WEI-SHIUNG YANG |
| 臺大學術典藏 |
2018-09-10T14:50:37Z |
Genetic Analysis of CARD14 in Non-familial Pityriasis Rubra Pilaris: A Case Series.
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TSEN-FANG TSAI;Tsai, Tsen-Fang;PEI-LUNG CHEN;Chen, You-Tzung;Jin-Bon Hong;Chen, Pei-Lung;Hong, Jin-Bon;You-Tzung Chen; You-Tzung Chen; Hong, Jin-Bon; JIN-BON HONG; PEI-LUNG CHEN; Tsai, Tsen-Fang |
| 臺大學術典藏 |
2018-09-10T09:42:02Z |
Tuberous sclerosis complex surveillance and management: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference.
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PEI-LUNG CHEN; Pei-Lung Chen |
| 臺大學術典藏 |
2018-09-10T09:42:02Z |
Tuberous sclerosis complex diagnostic criteria update: recommendations of the 2012 Iinternational Tuberous Sclerosis Complex Consensus Conference.
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Pei-Lung Chen; PEI-LUNG CHEN |
| 臺大學術典藏 |
2018-09-10T09:38:42Z |
Gene-wide tagging study of the effects of common genetic polymorphisms in the α subunits of the GABAA receptor on epilepsy treatment response
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Hung, C.-C.;Chen, P.-L.;Huang, W.-M.;Tai, J.J.;Hsieh, T.-J.;Ding, S.-T.;Hsieh, Y.-W.;Liou, H.-H.; Hung, C.-C.; Chen, P.-L.; Huang, W.-M.; Tai, J.J.; Hsieh, T.-J.; Ding, S.-T.; Hsieh, Y.-W.; Liou, H.-H.; SHIH-TORNG DING; PEI-LUNG CHEN |
| 臺大學術典藏 |
2018-09-10T09:38:42Z |
Identification of a novel HLA-B allele, B*07:162, in a Taiwanese individual
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Chen, P.-L.;Lai, S.-K.;Yang, W.-S.;Chang, T.-C.;Chu, C.-C.; TIEN-CHUN CHANG; WEI-SHIUNG YANG; PEI-LUNG CHEN |
| 臺大學術典藏 |
2018-09-10T09:12:57Z |
An isodicentric X chromosome with gonadal dysgenesis in a lady without prominent somatic features of Turner's syndrome. A case report
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Yu, T.-Y.;Lin, H.-S.;Chen, P.-L.;Huang, T.-S.; PEI-LUNG CHEN; TIEN-SHANG HUANG |
| 臺大學術典藏 |
2018-09-10T09:12:57Z |
Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas
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Wang, C.-P. and Chen, T.-C. and Chang, Y.-L. and Ko, J.-Y. and Yang, T.-L. and Lo, F.-Y. and Hu, Y.-L. and Chen, P.-L. and Wu, C.-C. and Lou, P.-J.; YIH-LEONG CHANG; TSUNG-LIN YANG; CHENG-PING WANG; PEI-LUNG CHEN; CHEN-CHI WU; PEI-JEN LOU |
| 臺大學術典藏 |
2018-09-10T08:28:22Z |
Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles
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Chen, P.-L.; Fann, C.-S.-J.; Chu, C.-C.; Chang, C.-C.; Chang, S.-W.; Hsieh, H.-Y.; Lin, M.; Yang, W.-S.; Chang, T.-C.; TIEN-CHUN CHANG; WEI-SHIUNG YANG; PEI-LUNG CHEN; CHEN, PEI-LUNG; FANN, CATHY SHENG-JIUAN; CHU, CHEN- CHUNG; CHANG, CHIEN-CHING; CHANG, SU-WEI; HSIEH, HSIN-YI; LIN, CHU-MARIE; YANG, WEI-SHIUNG; CHANG, TIEN-CHUN |
| 臺大學術典藏 |
2018-09-10T08:28:22Z |
Linkage and association on 8p21.2-p21.1 in schizophrenia
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Fallin, M.D. Lasseter, V.K. Liu, Y. Avramopoulos, D. Mcgrath, J. Wolyniec, P.S. Nestadt, G. Liang, K.-Y. Chen, P.-L. Valle, D. Pulver, A.E.; PEI-LUNG CHEN |
顯示項目 141-150 / 156 (共16頁)
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