Author:
Albrecht Urs,Sutcliffe James S.,Cattanach Bruce M.,Beechey Colin V.,Armstrong Dawna,Eichele Gregor,Beaudet Arthur L.
Publisher
Springer Science and Business Media LLC
Reference23 articles.
1. Nicholls, R.D. New insights reveal complex mechanisms involved in genomic imprinting. Am. J. Hum. Genet. 54, 733–740 (1994).
2. Ledbetter, D.H., Ballabio, A. Molecular cytogenetics of contiguous gene syndromes: mechanisms and consequences of gene dosage imbalance. in The Metabolic and Molecular Bases of Inherited Disease, 7th ed. (eds Scriver, C.R., Beaudet, A.L., Sly, W.S. & Valle, D.) 811–839 (McGraw-Hill, New York, 1995).
3. Williams, C.A. et al. Angelman syndrome. Curr. Probl. Pediatr. 25, 216–231 (1995).
4. Buiting, K. et al. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nature Genet. 9, 395–400 (1995).
5. Matsuura, T. et al. De novo truncating mutations in E6-AP ubiquitin–protein ligase gene (UBE3A) in Angelman syndrome. Nature Genet. 15, 74–77 (1997).
Cited by
434 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