FMR1 and fragile X syndrome: 20 Hantash Hantash FM FM Goos Goos DG DG Tsao Tsao D D et al et al Qualitative assessment of FMR1 (CGG)n triplet repeat status in normal, intermediate, premutation, full mutation, and mosaic carriers in both sexes: Implications for fragile X syndrome carrier and newborn screening Qualitative assessment of FMR1 (CGG)n triplet repeat status in normal, intermediate, premutation, full mutation, and mosaic carriers in both sexes: Implications for fragile X syndrome carrier and newborn screening Genet Med Genet Med 2010 2010 10.1097/GIM.0b013e3181d0d40e 10.1097/GIM.0b013e3181d0d40e