1. Adelaide Research & Scholarship

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Results 1-10 of 33 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1998Concept mapping: How should it be introduced, and is there evidence for long term benefit?Santhanam, E.; Leach, Carolyn R.; Dawson, Chris J.
1998The acetylation patterns of histones H3 and H4 along Vicia faba chromosomes are differentBelyaev, Nikolai D.; Houben, Andreas; Baranczewski, Pawel; Schubert, Ingo
1998Decapentaplegic is required for arrest in G1 phase during Drosophila eye developmentHorsfield, Julie A.; Penton, Andrea; Secombe, Julie; Hoffman, F. Michael; Richardson, Helena Elizabeth
1998A very high density microsatellite map (1 STR/41kb) of 1.7 Mb on Xp22 spanning the microphthalmia with linear skin defects (MLS) syndrome critical regionCox, Timothy C.; Cox, Liza L.; Ballabio, Andrea
1998Embryonic globins of the marsupial the Tammar Wallaby (Macropus Eugenii): bird like and mammal like.Holland, Robert A.; Gooley, Andrew A.; Hope, Rory M.
1998B-chromosome origin in the endemic New Zealand frog Leiopelma hochstetteri through sex chromosome devolution.Sharbel, Timothy F.; Green, David M.; Houben, Andreas
1998A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy.Donnelly, A.; Haan, E.; Manson, J.; Mulley, J.
1998Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24Phillips, H.; Scheffer, I.; Crossland, K.; Bhatia, K.; Fish, D.; Marsden, C.; Howell, S.; Stephenson, J.; Tolmie, J.; Plazzi, G.; Eeg-Olofsson, O.; Singh, R.; Lopes-Cendes, I.; Andermann, E.; Berkovic, S.; Mulley, J.
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.
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.

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