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PreviewIssue DateTitleAuthor(s)
1999Evolution and molecular characterization of a β-globin gene from the Australian Echidna Tachyglossus aculeatus (Monotremata)Lee, M.; Shroff, R.; Cooper, S.; Hope, R.
1999Systematic relationships within the Dasyurid Marsupial Tribe Sminthopsini - a multigene approachBlacket, M.; Krajewski, C.; Labrinidis, A.; Cambron, B.; Cooper, S.; Westerman, M.
1999Genomic structure and expression analysis of the spastic paraplegia gene, SPG7Settasatian, C.; Whitmore, S.; Crawford, J.; Bilton, R.; Cleton-Jansen, A.; Sutherland, G.; Callen, D.
1998Characterisation and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancerWhitmore, S.; Settasatian, C.; Crawford, J.; Lower, K.; McCallum, B.; Seshadri, R.; Cornelisse, C.; Moerland, E.; Cleton-Jansen, A.; Tipping, A.; Mathew, C.; Savnio, M.; Savoia, A.; Verlander, P.; Auerbach, A.; Van Berkel, C.; Pronk, J.; Doggett, N.; Callen, D.
1998The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.Kortschak, R.; Reimann, H.; Zimmer, M.; Eyre, H.; Saint, R.; Jenne, D.
1995Ectopic cyclin E expression induces premature entry into S phase and disrupts pattern formation in the Drosophila eye imaginal discRichardson, H.; O'Keefe, L.; Marty, T.; Saint, R.
1999Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3Cleton-Jansen, A.; Moerland, E.; Pronk, J.; Van Berkel, C.; Apostolou, S.; Crawford, J.; Savoia, A.; Auerbach, A.; Callen, D.; Cornelisse, C.
1996Analysis of mutations in the creA gene involved in carbon catabolite repression in Aspergillus nidulansShroff, R.; Lockington, R.; Kelly, J.
1996Refinement of the background genetic map of Xq26-q27 and gene localisation for Borjeson-Forssman-Lehmann syndromeGedeon, A.; Kozman, H.; Robinson, H.; Pilia, G.; Schlessinger, D.; Turner, G.; Mulley, J.
1996Regional localisation of two non-specific X-linked mental retardation genes (MRX 30 and MRX 31)Donnelly, A.; Partington, M.; Ryan, A.; Mulley, J.