1. Adelaide Research & Scholarship

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Results 31-40 of 46 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1996A novel X-linked gene, G4.5. is responsible for Barth SyndromeBione, S.; D'Adamo, P.; Maestrini, E.; Gedeon, A.; Bolhuis, P.; Toniolo, D.
1996Identification of the gene FMR2, associated with FRAXE mental retardationGecz, J.; Gedeon, A.; Sutherland, G.; Mulley, J.
1998Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16Cavanaugh, J.; Callen, D.; Wilson, S.; Stanford, P.; Sraml, M.; Gorska, M.; Crawford, J.; Whitmore, S.; Shlegel, C.; Foote, S.; Kohonen-Corish, M.; Pavli, P.
1998A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis.Town, M.; Jean, G.; Cherqui, S.; Attard, M.; Forestier, L.; Whitmore, S.; Callen, D.; Gribouval, O.; Broyer, M.; Bates, G.; van't Hoff, W.; Antignac, C.
1997The influence of muscle blood flow on fatigue during intermittent human hand-grip exercise and recoveryPitcher, J.; Miles, T.
1995Influence of handedness on motor unit discharge properties and physiological tremorSemmler, J.; Nordstrom, M.
1995FRAXE and mental retardationMulley, J.; Yu, S.; Loesch, D.; Hay, D.; Donnelly, A.; Gedeon, A.; Carbonell, P.; Lopez, I.; Glover, G.; Garbarron, I.; Yu, P.; Baker, E.; Haan, E.; Hockey, A.; Knight, S.; Daview, K.; Richards, R.; Sutherland, G.
1999Effect of vitamin C supplementation on chromosome damage, apoptosis and necrosis ex vivoCrott, J.; Fenech, M.
1998PAK3 mutation in nonsyndromic X-linked mental retardationAllen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
1999Genomic organisation and biological characterization of the novel human CC chemokine DC-CK-1/PARC/MIP-4/SCYA18Guan, P.; Burghes, A.; Cunningham, A.; Lira, P.; Brissette, W.; Neote, K.; McColl, S.

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