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Results 11-19 of 19 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1995Apert syndrome results from localised mutations of FGFR2 and is allelic with Crouzon syndromeWilkie, A.; Slaney, S.; Oldridge, M.; Poole, M.; Ashworth, G.; Hockley, A.; Hayward, R.; David, D.; Pulleyn, L.; Rutland, P.; Malcolm, S.; Winter, R.; Reardon, W.
1995Sequence, genomic organization and expression of the novel homeobox gene Hesx1THOMAS, P.; JOHNSON, B.; RATHJEN, J.; RATHJEN, P.
1995Genetic rearrangements in the rfb regions of Vibrio cholerae O1 and O139Stroeher, U.; Dredge, B.; Morona, R.; Brown, M.; Karageorgos, L.; Albert, M.; Manning, P.
1995A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathyLaing, N.; Wilton, S.; Akkari, P.; Dorosz, S.; Boundy, K.; Kneebone, C.; Blumbergs, P.; White, S.; Watkins, H.; Love, D.; Haan, E.
1995Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndromeScott, H.; Blanch, L.; Guo, X.H.; Freeman, C.; Orsborn, A.; Baker, E.; Sutherland, G.; Morris, C.; Hopwood, J.
1995A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsySteinlein, O.; Mulley, J.; Propping, P.; Wallace, R.; Phillips, H.; Sutherland, G.; Scheffer, I.; Berkovic, S.
1995Molecular cloning of the cDNA encoding human skeletal muscle triadin and its localisation to chromosome 6q22-6q23Taske, N.; Eyre, H.; O'Brien, R.; Sutherland, G.; Denborough, M.; Foster, P.
1995Bovine latent transforming growth factor β1-binding protein 2: molecular cloning, identification of tissue isoforms, and immunolocalization to elastin-associated microfibrilsGibson, M.; Hatzinikolas, G.; Davis, E.; Baker, E.; Sutherland, G.; Mecham, R.
1995Cloning and sequence analysis of caprine N-acetylglucosamine 6-sulfatase cDNAFriderici, K.; Cavanagh, K.; Leipprandt, J.; Traviss, C.; Anson, D.; Hopwood, J.; Jones, M.

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