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PreviewIssue DateTitleAuthor(s)
1997High resolution characterisation of an interstitial deletion of less than 1.9Mb at 4p16.3 associated with Wolf-Hirschhorn SyndromeFang, Y.; Bain, S.; Haan, E.; Eyre, H.; MacDonald, M.; Wright, T.; Altherr, M.; Riess, O.; Sutherland, G.; Callen, D.
1995The human OTF1 locus which overlaps the CD3Z gene is located at 1q22>q23Sturm, R.; Eyre, H.; Baker, E.; Sutherland, G.
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.
1999GPR56, a novel secretin-like human G-protein-coupled receptor geneLiu, M.; Parker, R.; Darby, K.; Eyre, H.; Copeland, N.; Crawford, J.; Gilbert, D.; Sutherland, G.; Jenkins, N.; Herzog, H.
1996Chromosomal mapping of the gene (P19) encoding the intracellular serpin proteinase inhibitor 9 to 6p25 By fluorescence in situ hybridizationEyre, H.; Sun, J.; Sutherland, G.; Bird, P.
1999Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardationGecz, J.; Barnett, S.; Liu, J.; Hollway, G.; Donnelly, A.; Eyre, H.; Eshkevari, H.; Baltazar, R.; Grunn, A.; Nagaraja, R.; Gilliam, C.; Peltonen, L.; Sutherland, G.; Baron, M.; Mulley, J.
1997Assignment of the Y-4 Receptor Gene (PPYR1) to Human Chromosome 10q11.2 and Mouse Chromosome 14Darby, K.; Eyre, H.; Lapsys, N.; Copeland, N.; Gilbert, D.; Couzens, M.; Antonova, O.; Sutherland, G.; Jenkins, N.; Herzog, H.

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