Adelaide Research & Scholarship
Browsing "School of Medicine" by Author Ha, T.T.
Showing results 1 to 3 of 3
Preview | Issue Date | Title | Author(s) |
| 2023 | Aicardi Syndrome Is a Genetically Heterogeneous Disorder | Ha, T.T.; Burgess, R.; Newman, M.; Moey, C.; Mandelstam, S.A.; Gardner, A.E.; Ivancevic, A.M.; Pham, D.; Kumar, R.; Smith, N.; Patel, C.; Malone, S.; Ryan, M.M.; Calvert, S.; van Eyk, C.L.; Lardelli, M.; Berkovic, S.F.; Leventer, R.J.; Richards, L.J.; Scheffer, I.E.; et al. |
| 2023 | Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis | Ghaoui, R.; Ha, T.T.; Kerkhof, J.; McConkey, H.; Gao, S.; Babic, M.; King, R.; Ravenscroft, G.; Kocyzek, B.; Otto, S.; Laing, N.G.; Scott, H.; Sadikovic, B.; Kassahn, K.S. |
| 2023 | Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death | Byrne, A.B.; Arts, P.; Ha, T.T.; Kassahn, K.S.; Pais, L.S.; O'Donnell-Luria, A.; Broad Institute Center for Mendelian Genomics,; Babic, M.; Frank, M.S.B.; Feng, J.; Wang, P.; Lawrence, D.M.; Eshraghi, L.; Arriola, L.; Toubia, J.; Nguyen, H.; Genomic Autopsy Study Research Network,; McGillivray, G.; Pinner, J.; McKenzie, F.; et al. |