22q11.2 deletion syndrome (22q11DS), a copy number variation (CNV) disorder, occurs in approximately 1:4000 live births due to a heterozygous microdeletion at position 11.2 (proximal) on the q arm of human chromosome 22 (hChr22) (McDonald-McGinn and Sullivan, Medicine 90:1-18, 2011)....
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Interestingly, a majority of the DNMT1W796A-related hypo-DMRs were found localized within the LINE-1 class of retrotransposon elements (also known as L1; Fig.4fand Supplementary Fig.6a), especially the 5′cis-regulatory region of a newly evolved, non-truncated L1MdA subfamily (Fig.4g, hand...
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SR10_0.2-1% 713 THV15_A150M_0.25_10 714 LM2825HN_ADJ NSC 715 12AV150 Pico 716 24VV1 Pico 717 T912_A100K_010_02 Caddock 718 7242-MA Penn Engineering 719 7342-MA Penn Engineering 720 4642-MMA5U Penn Engineering 721 4642-MMA2U Penn Engineering 722 148-90-40-2-SMA-F-C-T1-0 UB...
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