1. The high prevalence of the fra(X) syndrome cannot be explained by a high mutation rate;Smits, A.; Smeets, D.; Hamel, B.; Dreesen, J.; van Oost, B.;Am J Med Genet,1992
2. Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the transmitting mcaalrer.ieAr mmoJthMeer, d and presence of a normal Genet;Smits, A.; van Oost, B.A.; de Haan, A.F.J.; Hamel, B.C.J.; Dreesen, J.C.F.M.; Smeets, D.C.F.M.,1992
3. Characterization of a proximal highly polymorphic to the fragile X dsiinteu.cleAotmideJ repeat;Riggins, G.J.; Sherman, S.L.; Oostra, B.A.;Med 150 kb Genet,1992
4. 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
5. 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.; Pizutti, A.;Cell,1991