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Results 1-10 of 30 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1995Fragile X syndrome and other dynamic mutation diseasesSutherland, G.; Richards, R.
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.
1995The genes encoding the myeloid nuclear differentiation antigen (MNDA) and IFI 16 are closely linked on human chromosome 1q22 but exhibit contrasting expression in haemopoietic cell lnesDawson, M.; Trapani, J.; Briggs, R.; Nicholl, J.; Sutherland, G.; Baker, E.
1995Gene duplication of the human peptide YY gene (PYY) generated the pancreatic polypeptide gene (PPY) on chromosome 17q21.1Hort, Y.; Baker, E.; Sutherland, G.; Shine, J.; Herzog, H.
1995Chromosomal mapping of the human proteinase inhibitor 6 (PI6) gene to 6p25 by fluorescence in situ hybridizationCoughlin, P.; Nicholl, J.; Sun, J.; Salem, H.; Bird, P.; Sutherland, G.
1995Assignment of the human neuropeptide Y gene to chromosome 7p15.1 by nonisotopic in situ hybridizationBaker, E.; Hort, Y.; Ball, H.; Sutherland, G.; Shine, J.; Herzog, H.
1995Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a 'hot-spot' for recombination at 16p12Callen, D.; Lane, S.; Kozman, H.; Kremmidiotis, G.; Whitmore, S.; Lowenstein, M.; Doggett, N.; Kenmochi, N.; Page, D.; Maglott, D.; Nierman, W.; Murakawa, K.; Sikela, J.; Houlgatte, R.; Auffray, C.; Sutherland, G.
1995Assignment of the gene encoding human galanin receptor (GALNR) to 18q23 by in situ hybridisationNicholl, J.; Kofler, B.; Sutherland, G.; Shine, J.; Iismaa, T.
1995The molecular basis of fragile sites in human chromosomesSutherland, G.; Richards, R.
1995Paracentric inversions do not normally generate monocentric recombinant chromosomesSutherland, G.; Callen, D.; McKinlay Gardner, R.