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显示项目 460901-460910 / 2348487 (共234849页)
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| 臺大學術典藏 |
2020-07-03T08:28:35Z |
Haplotype frequencies of nine Y-chromosome STR loci in the Taiwanese Han population
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Tsai L.-C.;Yuen T.-Y.;Hsieh H.-M.;Lin M.;Tzeng C.-H.;Huang N.-E.;Linacre A.;James Chun-I Lee; Tsai L.-C.; Yuen T.-Y.; Hsieh H.-M.; Lin M.; Tzeng C.-H.; Huang N.-E.; Linacre A.; JAMES CHUN-I LEE |
| 國立臺灣大學 |
2013 |
Haplotype Kernel Association Test as a Powerful Method to Identify Chromosomal Regions Harboring Uncommon Causal Variants
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Lin, Wan-Yu; Yi, Nengjun; Lou, Xiang-Yang; Zhi, Degui; Zhang, Kui; Gao, Guimin; Tiwari, Hemant K.; Liu, Nianjun; 林菀俞 |
| 臺大學術典藏 |
2018-09-10T09:41:02Z |
Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants
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Lin, Wan-Yu;Yi, Nengjun;Lou, Xiang-Yang;Zhi, Degui;Zhang, Kui;Gao, Guimin;Tiwari, Hemant K.;Liu, Nianjun; Lin, Wan-Yu; WAN-YU LIN; Yi, Nengjun; Lou, Xiang-Yang; Zhi, Degui; Zhang, Kui; Gao, Guimin; Tiwari, Hemant K.; Liu, Nianjun |
| 臺大學術典藏 |
2022-05-04T09:10:39Z |
Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants
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WAN-YU LIN; Yi N.; Lou X.-Y.; Zhi D.; Zhang K.; Gao G.; Tiwari H.K.; Liu N. |
| 中國醫藥大學 |
2010-06 |
Haplotype of BAK1 (BCL2 antagonist killer 1) polymorphisms associated with the risk of developing Kawasaki disease in Taiwanese children
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黃毓銓(Yu-Chuen Huang);林應如(Ying-Ju Lin);張正成(Jeng-Sheng Chang);陳世殷(Shih-Yin, Chen);萬磊(Lei Wan);許晉銓(Jinn-Chyuan Sheu);賴志河(Chih-Ho Lai);林振文(Lin Cheng Wen);劉詩平(Shih-Ping Liu);蔡輔仁(Fuu-Jen Tsai)* |
| 高雄醫學大學 |
2007 |
Haplotype Tag SNP Selection using Hybrid Algorithms
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Yang, Cheng-Hong;Ho, Chang-Hsuan;谷德倫;張學偉 |
| 高雄醫學大學 |
2008 |
Haplotype Tagging SNPs Selection Using Particle Swarm Optimization
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Yang, Cheng-Hong;Ho, Chang-Hsuan;張學偉;Chuang , Li-Yeh |
| 國立臺灣大學 |
2012 |
Haplotype-Based Methods for Detecting Uncommon Causal Variants With Common SNPs
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Lin, Wan-Yu; Yi, Nengjun; Zhi, Degui; Zhang, Kui; Gao, Guimin; Tiwari, Hemant K.; Liu, Nianjun; 林菀俞 |
| 臺大學術典藏 |
2022-05-04T09:10:40Z |
Haplotype-Based Methods for Detecting Uncommon Causal Variants With Common SNPs
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WAN-YU LIN; Yi N.; Zhi D.; Zhang K.; Gao G.; Tiwari H.K.; Liu N. |
| 國家衛生研究院 |
2019-07 |
Haplotypes constructed by Whole exome sequencing to map and identify a novel disease-causing RP2 gene variant from a recessive X linked Retinities Pigmentosa family
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Ching, Y;Fan, W;Lin, W;Tsai, W;Hu, L;Huang, S;Chung, R |
显示项目 460901-460910 / 2348487 (共234849页)
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