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PreviewIssue DateTitleAuthor(s)
1997Genomic structure and complete nucleotide sequence of the Batten Disease Gene, CLN3Mitchison, H.; Munroe, P.; O'Rawe, A.; Taschner, P.; De Vos, N.; Kremmidiotis, G.; Lensink, I.; Munk, A.; D'Arigo, K.; Anderson, J.; Lerner, T.; Moyzis, R.; Callen, D.; Breuning, M.; Doggett, N.; Gardiner, R.; Mole, S.
1998Construction of an ~700-kb transcript map around the Familial Mediterranean Fever locus on human chromosome 16p13.3Centola, M.; Chen, X.; Sood, R.; Deng, Z.; Aksentijevich, I.; Blake, T.; Ricke, D.; Chen, X.; Wood, G.; Zaks, N.; Richards, N.; Krizman, D.; Mansfield, E.; Apostolou, S.; Liu, J.; Shafran, N.; Vedula, A.; Hamon, M.; Cercek, A.; Kahan, T.; et al.
1997Mechanism of bacteriophage SfII-mediated sertype conversion in Shigella flexneriMavris, M.; Manning, P.; Morona, R.
1996The molecular organisation of a B chromosome tandem repeat sequence from Brachycome dichromosomaticaFranks, T.; Houben, A.; Leach, C.; Timmis, J.
1999The Shigella flexneri bacteriophage Sf6 tailspike protein (TSP)/endorhamnosidase is related to the bacteriophage P22 TSP and has a motif common to exo- and endoglycanases, and C-5 epimerasesChua, J.; Manning, P.; Morona, R.
1998Inactivation of two haemolytic toxin genes in Aeromonas hydrophila attenuates virulence in a suckling mouse modelWong, C.; Heuzenroeder, M.; Flower, R.
1998PAK3 mutation in nonsyndromic X-linked mental retardationAllen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
1999Evolution and molecular characterization of a β-globin gene from the Australian Echidna Tachyglossus aculeatus (Monotremata)Lee, M.H.; Shroff, R.; Cooper, S.; Hope, R.
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.M.; 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.

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