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Yeun Jun Chung 7 Articles
Comparison of the Affymetrix SNP Array 5.0 and Oligoarray Platforms for Defining CNV.
Ji Hong Kim, Seung Hyun Jung, Hae Jin Hu, Seon Hee Yim, Yeun Jun Chung
Genomics Inform. 2010;8(3):138-141.
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No Association between Copy Number Variation of the TCRB Gene and the Risk of Autism Spectrum Disorder in the Korean Population.
So Young Yang, Seon Hee Yim, Hae Jin Hu, Soon Ae Kim, Hee Jeong Yoo, Yeun Jun Chung
Genomics Inform. 2010;8(2):76-80.
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Replication of the Association between Copy Number Variation on 8p23.1 and Autism by Using ASD-specific BAC Array.
Jung Hoon Woo, Song Ju Yang, Seon Hee Yim, Hae Jin Hu, Myung Ju Shin, Eun Hee Oh, Hyun Woong Kang, Seonyang Park, Yeun Jun Chung
Genomics Inform. 2010;8(1):19-27.
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Comparison of Normalization Methods for Defining Copy Number Variation Using Whole-genome SNP Genotyping Data.
Ji Hong Kim, Seon Hee Yim, Yong Bok Jeong, Seong Hyun Jung, Hai Dong Xu, Seung Hun Shin, Yeun Jun Chung
Genomics Inform. 2008;6(4):231-234.
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CGHscape: A Software Framework for the Detection and Visualization of Copy Number Alterations.
Yong Bok Jeong, Tae Min Kim, Yeun Jun Chung
Genomics Inform. 2008;6(3):126-129.
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Copy Number Variations in the Human Genome: Potential Source for Individual Diversity and Disease Association Studies.
Tae Min Kim, Seon Hee Yim, Yeun Jun Chung
Genomics Inform. 2008;6(1):1-7.
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Current Status and Future Clinical Applications of Array.based Comparative Genomic Hybridization.
Seon Hee Yim, Yeun Jun Chung
Genomics Inform. 2004;2(3):113-120.
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