Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference63 articles.
1. Abyzov A, Li S, Kim DR, Mohiyuddin M, Stütz AM, Parrish NF et al. (2015) Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms. Nat Commun 6:7256
2. Anand R, Villasante A, Tyler-Smith C (1989) Construction of yeast artificial chromosome libraries with large inserts using fractionation by pulsed-field gel electrophoresis. Nucleic Acids Res 17:3425–3433
3. Berget SM, Moore C, Sharp PA (1977) Spliced segments at the 5’ terminus of adenovirus 2 late mRNA. Proc Natl Acad Sci USA 74:3171–3175
4. Bhatia S, Bengani H, Fish M, Brown A, Divizia MT, de Marco R et al. (2013) Disruption of autoregulatory feedback by a mutation in a remote, ultraconserved PAX6 enhancer causes aniridia. Am J Hum Genet 93:1–9
5. Bhatia S, Gordon CT, Foster RG, Melin L, Abadie V, Baujat G et al. (2015) Functional assessment of disease-associated regulatory variants in vivo using a versatile dual colour transgenesis strategy in zebrafish. PLoS Genet 11:e1005193
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献