Author:
Trent R J,Sheffield L J,Deng Z M,Kim W S,Nassif N T,Ryce C,Woods C G,Michaelis R C,Tarleton J,Smith A
Subject
Genetics (clinical),Genetics
Reference13 articles.
1. American Society of Human Genetics/American College of Medical Genetics Test and Technology Transfer Committee. Diagnostic testing for Prader-Willi and Angelman sydndromes: report of the ASHG/ACMG test and technology transfer committee;Am Hum Genet,1996
2. UBE3A/E6-AP mutations cause Angelman syndrome;Kishino, T.; Lalande, M.; Wagstaff, J.;Nat Genet,1997
3. De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome;Matsuura, T.; Sutcliffe, J.S.; Fang, P.;Nat Genet,1997
4. The ubiquitin-proteasome proteolytic pathway;Ciechanover, A.;Cell,1994
5. Deletion involving D 15S 113 in a mother and son without Angelman syndrome: refinement of the Angelman syndrome critical deletion region;Michaelis, R.C.; Skinner, S.A.; Lethco, B.A.;Am Med Genet,1995
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