1. Identification of a gene (FMR1) 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
2. Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation;Rousseau, F.; Heitz, D.; Biancalana, V.;N Engl Jf Med,1991
3. The fragile X syndrome: recent developments;Turk, J.;Current Opinion in Psychiatry,1992
4. The fragile X syndrome;Turk, J.; Hagerman, R.J.; Barnicoat, A.; McEvoy, J.,1994
5. Girls with fragile X syndrome: physical and neurocognitive status and outcome;Hagerman, R.J.; Jackson, C.; Amiri, K.; Cronister-Silverman, A.; O'Connor, R.; Sobesky, W.;Pediatrics,1992