Author:
Morton J E,Bundey S,Webb T P,MacDonald F,Rindl P M,Bullock S
Subject
Genetics (clinical),Genetics
Reference24 articles.
1. The frequency of the fragile X chromosome among schoolchildren in Coventry;Webb, T.P.; Bundey, S.; Thake, A.; Todd, J.;J Med Genet,1986
2. The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X;Sutherland, G.R.; Baker, E.;Clin Genet,1990
3. Instability of a 550- base pair DNA segment and abnormal methylation in fragile X syndrome;Oberle, I.; Rousseau, F.; Heitz, D.;Science,1991
4. Fragile X genotype characterised by an unstable region of DNA;Yu, S.; Pritchard, M.; Kremer, E.;Science,1991
5. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk, A.J.M.H.; Pieretti, M.; Sutcliffe, J.S.;Cell,1991
Cited by
72 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