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Estimation of DNA contamination and its sources in genotyped samples.
Zajac GJM, Fritsche LG, Weinstock JS, Dagenais SL, Lyons RH, Brummett CM, Abecasis GR. Zajac GJM, et al. Among authors: dagenais sl. Genet Epidemiol. 2019 Dec;43(8):980-995. doi: 10.1002/gepi.22257. Epub 2019 Aug 26. Genet Epidemiol. 2019. PMID: 31452258 Free PMC article.
Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.
Butler MG, Dagenais SL, Garcia-Perez JL, Brouillard P, Vikkula M, Strouse P, Innis JW, Glover TW. Butler MG, et al. Among authors: dagenais sl. Am J Med Genet A. 2012 Apr;158A(4):839-49. doi: 10.1002/ajmg.a.35229. Epub 2012 Mar 9. Am J Med Genet A. 2012. PMID: 22407726 Free PMC article.
A novel VEGFR3 mutation causes Milroy disease.
Butler MG, Dagenais SL, Rockson SG, Glover TW. Butler MG, et al. Among authors: dagenais sl. Am J Med Genet A. 2007 Jun 1;143A(11):1212-7. doi: 10.1002/ajmg.a.31703. Am J Med Genet A. 2007. PMID: 17458866 Free article.
Mutation of the FOXC2 gene in familial distichiasis.
Brooks BP, Dagenais SL, Nelson CC, Glynn MW, Caulder MS, Downs CA, Glover TW. Brooks BP, et al. Among authors: dagenais sl. J AAPOS. 2003 Oct;7(5):354-7. doi: 10.1016/s1091-8531(03)00144-7. J AAPOS. 2003. PMID: 14566319
Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations.
Erickson RP, Dagenais SL, Caulder MS, Downs CA, Herman G, Jones MC, Kerstjens-Frederikse WS, Lidral AC, McDonald M, Nelson CC, Witte M, Glover TW. Erickson RP, et al. Among authors: dagenais sl. J Med Genet. 2001 Nov;38(11):761-6. doi: 10.1136/jmg.38.11.761. J Med Genet. 2001. PMID: 11694548 Free PMC article.
21 results