Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome

Eichler EE, Macpherson JN, Murray A, Jacobs PA, Chakravarti A, Nelson DL. (1996). Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome. Hum Mol Genet Mar;5(3):319-330.