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Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogenetics.
Dong Z, Wang H, Chen H, Jiang H, Yuan J, Yang Z, Wang WJ, Xu F, Guo X, Cao Y, Zhu Z, Geng C, Cheung WC, Kwok YK, Yang H, Leung TY, Morton CC, Cheung SW, Choy KW. Dong Z, et al. Among authors: wang h, wang wj. Genet Med. 2018 Jul;20(7):697-707. doi: 10.1038/gim.2017.170. Epub 2017 Nov 2. Genet Med. 2018. PMID: 29095815 Free PMC article.
Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach.
Dong Z, Zhang J, Hu P, Chen H, Xu J, Tian Q, Meng L, Ye Y, Wang J, Zhang M, Li Y, Wang H, Yu S, Chen F, Xie J, Jiang H, Wang W, Choy KW, Xu Z. Dong Z, et al. Among authors: wang h, wang w, wang j. Genet Med. 2016 Sep;18(9):940-8. doi: 10.1038/gim.2015.199. Epub 2016 Jan 28. Genet Med. 2016. PMID: 26820068 Free article.
Copy-Number Variants Detection by Low-Pass Whole-Genome Sequencing.
Dong Z, Xie W, Chen H, Xu J, Wang H, Li Y, Wang J, Chen F, Choy KW, Jiang H. Dong Z, et al. Among authors: wang h, wang j. Curr Protoc Hum Genet. 2017 Jul 11;94:8.17.1-8.17.16. doi: 10.1002/cphg.43. Curr Protoc Hum Genet. 2017. PMID: 28696555
Balanced Chromosomal Rearrangement Detection by Low-Pass Whole-Genome Sequencing.
Dong Z, Ye L, Yang Z, Chen H, Yuan J, Wang H, Guo X, Li Y, Wang J, Chen F, Cheung SW, Morton CC, Jiang H, Choy KW. Dong Z, et al. Among authors: wang h, wang j. Curr Protoc Hum Genet. 2018 Jan 24;96:8.18.1-8.18.16. doi: 10.1002/cphg.51. Curr Protoc Hum Genet. 2018. PMID: 29364520 Free PMC article.
150,054 results
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