Author:
Wohrle D,Salat U,Glaser D,Mucke J,Meisel-Stosiek M,Schindler D,Vogel W,Steinbach P
Subject
Genetics (clinical),Genetics
Reference35 articles.
1. Identification of a gene (FMR-1) containing a CGG repeat coincident illl with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk, A.J.M.H.; Pieretti, M.; Sutcliffe, J.S.;Cell,1991
2. Fragile X genotype characterized by an unstable region of DNA;YuS, Pritchard M.; E, Kremer;Science,1991
3. et al Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome;Oberil, I.; Rousseau, F.; Heitz, D.;Science,1991
4. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox;Fu, Y.H.; Kuhl, D.P.A.; Pizzutti, A.;Cell,1991
5. Methylation analysis of CGG sites in the CpG island of the human FMR1 gene;Hansen, R.S.; Gartler, S.M.; Scott, C.R.;Hum Mol Genet,1992
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