1. Adelaide Research & Scholarship

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Results 1-10 of 114 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
1997Mapping of the gene for vascular endothelial growth factor-D in mouse and man to the X chromosomeJenkins, N.; Woollatt, E.; Crawford, J.; Gilbert, D.; Baldwin, M.; Sutherland, G.; Copeland, N.; Achen, M.
2008X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentDibbens, L.; Tarpey, P.; Hynes, K.; Bayly, M.; Scheffer, I.; Smith, R.; Bomar, J.; Sutton, E.; Vandeleur, L.; Shoubridge, C.; Edkins, S.; Turner, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Jones, D.; et al.
1995Fragile X syndrome and other dynamic mutation diseasesSutherland, G.; Richards, R.
2004Nxf and Fbxo33: novel seizure-responsive genes in miceFlood, W.; Moyer, R.; Tsykin, A.; Sutherland, G.; Koblar, S.
2014Placental restriction of fetal growth reduces cutaneous responses to antigen after sensitization in sheepWooldridge, A.; Bischof, R.; Meeusen, E.; Liu, H.; Heinemann, G.; Hunter, D.; Giles, L.; Kind, K.; Owens, J.; Clifton, V.; Gatford, K.
2001Glucose-regulated insulin expression in diabetic ratsBarry, S.; Ramesh, N.; Lejnieks, D.; Simonson, W.; Kemper, L.; Lernmark, A.; Osborne, W.
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.
1995Assignment of the human skeletal muscle a-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridizationEyre, H.; Akkari, P.; Wilton, S.; Callen, D.; Baker, E.; Laing, N.
1996bcl-w, a novel member of the bcl-2 family, promotes cell survivalGibson, L.; Holmgreen, S.; Huang, D.; Bernand, O.; Copeland, N.; Jenkins, N.; Sutherland, G.; Baker, E.; Adams, J.; Cory, S.
1998Haemolytic-uraemic syndrome outbreak caused by Escherichia coli O111:H-: clinical outcomesHenning, P.; Tham, E.; Martin, A.; Beare, T.; Jureidini, K.

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