Browsing byAuthorSadedin, S
Showing results 1 to 2 of 2
| Issue Date | Title | Author(s) |
| 2017-05 | Diagnostic and cost utility of whole exome sequencing in peripheral neuropathy. | Walsh, M; Bell, KM; Chong, B; Creed, E; Brett, GR; Pope, K; Thorne, NP; Sadedin, S; Georgeson, P; Phelan, DG; Day, T; Taylor, JA; Sexton, A; Lockhart, PJ; Kiers, L; Fahey, M; Macciocca, I; Gaff, CL; Oshlack, A; Yiu, EM; James, PA; Stark, Z; Ryan, MM; Melbourne Genomics Health Alliance, |
| 2024 | Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns. | Alshawsh, M; Wake, M; Gecz, J; Corbett, M; Saffery, R; Pitt, J; Greaves, R; Williams, K; Field, M; Cheong, J; Bui, M; Arora, S; Sadedin, S; Lunke, S; Wall, M; Amor, DJ; Godler, DE |
