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Results 21-30 of 139 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1999Aquatic sex pheromone from a male tree frogWabnitz, P.; Bowie, J.; Tyler, M.; Wallace, J.; Smith, B.
1998Identification of a human HECT family protein with homology to the Drosophila tumor suppressor gene hyperplastic discsCallaghan, M.; Russell, A.; Woollatt, E.; Sutherland, G.; Sutherland, R.; Watts, C.
1997A Novel Epithelial-Expressed ETS Gene, ELF3 - Human and Murine cDNA Sequences, Murine Genomic Organization, Human Mapping to 1q32.2 and Expression in Tissues and CancerTymms, M.; Ng, A.; Thomas, R.; Schutte, B.; Zhou, J.; Eyre, H.; Sutherland, G.; Seth, A.; Rosenberg, M.; Papas, T.; Debouck, C.; Kola, I.
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.
1999Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tardaGedeon, A.; Colley, A.; Jamieson, R.; Thompson, E.; Rogers, J.; Sillence, D.; Tiller, G.; Mulley, J.; Gecz, J.
1998Protein synthesis and secretion by the epididymis of the brushtail possum, Trichosurus vulpeculaLamont, A.; Clarke, H.; Cooper, N.; Holland, M.; Breed, W.
1995Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisationHunt, C.; Eyre, H.; Akkari, P.; Meredith, C.; Dorosz, S.; Wilton, S.; Callen, D.; Laing, N.; Baker, E.
2015Single nucleotide variations in CLCN6 identified in patients with benign partial epilepsies in infancy and/or febrile seizuresYamamoto, T.; Shimojima, K.; Sangu, N.; Komoike, Y.; Ishii, A.; Abe, S.; Yamashita, S.; Imai, K.; Kubota, T.; Fukasawa, T.; Okanishi, T.; Enoki, H.; Tanabe, T.; Saito, A.; Furukawa, T.; Shimizu, T.; Milligan, C.; Petrou, S.; Heron, S.; Dibbens, L.; et al.; Ishii, R.
1996Characterisation of four novel fibrillin-1 mutations in the Marfan syndromeAdes, L.; Haan, E.; Colley, A.; Richards, R.
2014Refining analyses of copy number variation identifies specific genes associated with developmental delayCoe, B.; Witherspoon, K.; Rosenfeld, J.; van Bon, B.; Vulto-van Silfhout, A.; Bosco, P.; Friend, K.; Baker, C.; Buono, S.; Vissers, L.; Schuurs-Hoeijmakers, J.; Hoischen, A.; Pfundt, R.; Krumm, N.; Carvill, G.; Li, D.; Amaral, D.; Brown, N.; Lockhart, P.; Scheffer, I.; et al.

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