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Results 11-17 of 17 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1999Molecular and genetic characterization of the capsule biosynthesis locus of Streptococcus pneumoniae type 23FMorona, J.; Miller, D.; Coffey, T.; Vindurampulle, C.; Spratt, B.; Morona, R.; Paton, J.
1999Genomic structure and expression analysis of the spastic paraplegia gene, SPG7Settasatian, C.; Whitmore, S.; Crawford, J.; Bilton, R.; Cleton-Jansen, A.M.; Sutherland, G.; Callen, D.
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.
1997The Mouse Homeobox Gene, Gbx2: Genomic Organisation and Expression in Pluripotent Cells in Vitro and in VivoChapman, G.; Remiszewski, J.; Webb, G.; Schulz, T.; Bottema, C.; Rathjen, P.