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ECEL1 mutation causes fetal arthrogryposis multiplex congenita.
Dohrn N, Le VQ, Petersen A, Skovbo P, Pedersen IS, Ernst A, Krarup H, Petersen MB. Dohrn N, et al. Among authors: pedersen is. Am J Med Genet A. 2015 Apr;167A(4):731-43. doi: 10.1002/ajmg.a.37018. Epub 2015 Feb 23. Am J Med Genet A. 2015. PMID: 25708584
Hypermethylated DNA, a circulating biomarker for colorectal cancer detection.
Rasmussen SL, Krarup HB, Sunesen KG, Johansen MB, Stender MT, Pedersen IS, Madsen PH, Thorlacius-Ussing O. Rasmussen SL, et al. Among authors: pedersen is. PLoS One. 2017 Jul 10;12(7):e0180809. doi: 10.1371/journal.pone.0180809. eCollection 2017. PLoS One. 2017. PMID: 28700744 Free PMC article.
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