1. Adelaide Research & Scholarship

Search


Current filters:
Start a new search
Add filters:

Use filters to refine the search results.

 | 
Results 61-70 of 1209 (Search time: 0.003 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
2002Results of consecutive trials for children newly diagnosed with acute myeloid leukemia from the Australian and New Zealand Children's Cancer Study GroupO'Brien, T.; Russell, S.; Vowels, M.; Oswald, C.; Tiedemann, K.; Shaw, P.; Lockwood, L.; Teague, L.; Rice, M.; Marshall, G.
1997Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evidentWicking, C.; Shanley, S.; Smyth, I.; Gillies, S.; Negus, K.; Graham, S.; Suthers, G.; Haites, N.; Edwards, M.; Wainwright, B.; Chenevix Trench, G.
2008Current use of Australian snake antivenoms and frequency of immediate-type hypersensitivity reactions and anaphylaxisIsbister, G.; Brown, S.; MacDonald, E.; White, J.; Currie, B.
1999Testisin, a new human serine proteinase expressed by premeiotic testicular germ cells and lost in testicular germ cell tumorsHooper, J.; Nicol, D.; Dickinson, J.; Eyre, H.; Scarman, A.; Normyle, J.; Stuttgen, M.; Douglas, M.; Loveland, K.; Sutherland, G.; Antalis, T.
1996An outbreak of hemolytic uremic syndrome due to escherichia coli O157:H-: or was it?Goldwater, P.; Bettelheim, K.
2008Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoformSharma, S.; Burdon, K.; Dave, A.; Jamieson, R.; Yaron, Y.; Billson, F.; van Maldergem, L.; Lorenz, B.; Gecz, J.; Craig, J.
1996REPEAT OFFENDERS - SIMPLE REPEAT SEQUENCES AND COMPLEX GENETIC PROBLEMS [Review]Richards, R.; Sutherland, G.
2001A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriersWang, W.; Spurdle, A.; Kolachana, P.; Bove, B.; Modan, B.; Ebbers, S.; Suthers, G.; Tucker, M.; Kaufman, D.; Doody, M.; Tarone, R.; Daly, M.; Levavi, H.; Pierce, H.; Chetrit, A.; Yechezkel, G.; Chenevix-Trench, G.; Offit, K.; Godwin, A.; Struewing, J.
1997A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeMuenke, M.; Gripp, K.; McDonald-McGinn, D.; Gaudenz, K.; Whitaker, L.; Bartlett, S.; Markowitz, R.; Robin, N.; Nwokoro, N.; Mulvihill, J.; Losken, H.; Mulliken, J.; Guttmacher, A.; Wilroy, R.; Clarke, L.; Hollway, G.; Ades, L.; Haan, E.; Mulley, J.; Cohen, M.; et al.
2000New mutations in MID1 provide support for loss of function as the cause of X-linked Optiz syndromeCox, T.; Allen, L.; Cox, L.; Hopwood, B.; Goodwin, B.; Haan, E.; Suthers, G.

Discover