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Preview	Issue Date	Title	Author(s)
	1998	PAK3 mutation in nonsyndromic X-linked mental retardation	Allen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
	1999	Evolution and molecular characterization of a β-globin gene from the Australian Echidna Tachyglossus aculeatus (Monotremata)	Lee, M.H.; Shroff, R.; Cooper, S.; Hope, R.
	1996	Identification of Novel Alternatively Spliced Pyruvate Carboxylase mRNAs with Divergent 5' -Untranslated Regions Which Are Expressed in a Tissue-Specific Manner	Jitrapakdee, S.; Walker, M.; Wallace, J.
	1997	Characterization of the locus encoding the Streptococcus pneumoniae type 19F capsular polysaccharide biuosynthetic pathway	Morona, J.; Morona, R.; Paton, J.
	1998	Characterisation and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer	Whitmore, 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.
	1997	Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the Familial Mediterranean Fever Locus (MEFV) on chromosome 16p13.3	Sood, R.; Blake, T.; Aksentijevich, I.; Wood, G.; Chen, X.; Gardner, D.; Shelton, D.; Mangelsdorf, M.; Orsborn, A.; Pras, E.; Balow, J.; Centola, M.; Deng, Z.; Zaks, N.; Chen, X.; Richards, N.; Fischel-Ghodsian, N.; Rotter, J.; Pras, M.; Shohat, M.; et al.
	1997	The genome organisation of the Fanconi Anemia Group A (FAA) Gene	Ianzano, L.; d'Apolito, M.; Centra, M.; Savino, M.; Levran, O.; Auerbach, A.; Cleton-Jansen, A.M.; Doggett, N.; Pronk, J.; Tipping, A.; Gibson, R.; Mathew, C.; Whitmore, S.; Apostolou, S.; Callen, D.; Zelante, L.; Savoia, A.
	1997	Gene structure and subcellular localisation of FMR2, a member of a new family of putative transcription activators	Gecz, J.; Bielby, S.; Sutherland, G.; Mulley, J.
	1998	The 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.
	1996	Long-term protection against HIV-1 infection conferred by tat or rev antisense RNA was affected by the design of the retroviral vector	Peng, H.; Callison, D.; Li, P.; Burrell, C.