Person A/Pr Howard Slater National Health and Medical Research Council Viewed: [[ro.stat.viewed]] Click to explore relationships graph Help Related Grants and Projects $relation_to_title = []; $dupes = 0;?> Principal investigator of Characterization of a novel epigenetic boundary and long range epigenetic modifications specific to FMR1 expansion carriers with behavioural and cognitive disorders - implications for earlier diagnosis and treatment. (funded by National Health and Medical Research Council) Principal investigator of Implementation of a new, inexpensive and high-throughput Matrix Assisted Laser Desorption / Ionization _ Time Of Flight Mass Spectrometry test for superior detection of Fragile X Syndrome in targeted diagnostics and newborn population screening. (funded by National Health and Medical Research Council) Participant in Novel Fragile X Syndrome prevalence estimates in 100,000 Australian newborns, prognostic and health-economic outcomes: a retrospective newborn screening study (funded by National Health and Medical Research Council) Participant in Towards adequate national provision of genomic testing in pregnancy (funded by National Health and Medical Research Council) User Contributed Tags Login to tag this record with meaningful keywords to make it easier to discover Saved to MyRDA Save to MyRDA
Click to explore relationships graph Help Related Grants and Projects $relation_to_title = []; $dupes = 0;?> Principal investigator of Characterization of a novel epigenetic boundary and long range epigenetic modifications specific to FMR1 expansion carriers with behavioural and cognitive disorders - implications for earlier diagnosis and treatment. (funded by National Health and Medical Research Council) Principal investigator of Implementation of a new, inexpensive and high-throughput Matrix Assisted Laser Desorption / Ionization _ Time Of Flight Mass Spectrometry test for superior detection of Fragile X Syndrome in targeted diagnostics and newborn population screening. (funded by National Health and Medical Research Council) Participant in Novel Fragile X Syndrome prevalence estimates in 100,000 Australian newborns, prognostic and health-economic outcomes: a retrospective newborn screening study (funded by National Health and Medical Research Council) Participant in Towards adequate national provision of genomic testing in pregnancy (funded by National Health and Medical Research Council) User Contributed Tags Login to tag this record with meaningful keywords to make it easier to discover