Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening : a technical validation study
This work was supported by the Victorian government’s Operational Infrastructure Support Program, an NHMRC development grant (no. 1017263 to H.R.S. and D.E.G.), the E.W. Al Thrasher Award, USA (to H.R.S. and D.E.G.), a National Institute of Child Health and Human Development grant, USA (HD36071 to D.Z.L. and R.J.H.), Andrology Australia, and Monash University and in part by a grant from the South Carolina Department of Disabilities and Special Needs.