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PreviewIssue DateTitleAuthor(s)
1998Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1BWallace, R.; Wang, D.; Singh, R.; Scheffer, I.; George Jnr., A.; Phillips, H.; Saar, K.; Reis, A.; Johnson, E.; Sutherland, G.; Berkovic, S.; Mulley, J.
1998Pyruvate carboxylaseWallace, J.; Jitrapakdee, S.; Chapman-Smith, A.
1998Comparison of the levels of intra-specific genetic variation within Giardia muris and Giardia intestinalisAndrews, R.; Monis, P.; Ey, P.; Mayrhofer, G.
1998Transcriptional activation of Cytochrome P450 genes by different classes of chemical inducersDogra, S.; Whitelaw, M.; May, B.
1998Repression of basal transcription by vitamin D receptor: evidence for interaction of unliganded vitamin D receptor with two receptor interaction domains in rip13Δ1Dwivedi, P.; Muscat, G.; Bailey, P.; Omdahl, J.; May, B.
1998PAK3 mutation in nonsyndromic X-linked mental retardationAllen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
1998The identification and localisation of a human gene with sequence similarity to Polycomblike of Drosophila melanogasterCoulson, M.; Robert, S.; Eyre, H.; Saint, R.
1998Localisation of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13.1-qter, the NMDAR2A subunit gene to 16p13.2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24-q25 using somatic cell hybrid and radiation hybrid mapping panels.Kalsi, G.; Whiting, P.; Bourdelles, B.; Callen, D.; Barnard, E.; Gurling, H.
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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