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Results 1-10 of 11 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1995Mechanisms of small ring formation suggested by the molecular characterization of 2 small accessory ring chromosomes derived from chromosome 4Fang, Y.; Eyre, H.; Bohlander, S.; Estop, A.; McPherson, E.; Trager, T.; Riess, O.; Callen, D.
1999Testisin, a new human serine proteinase expressed by premeiotic testicular germ cells and lost in testicular germ cell tumorsHooper, J.; Nicol, D.; Dickinson, J.; Eyre, H.; Scarman, A.; Normyle, J.; Stuttgen, M.; Douglas, M.; Loveland, K.; Sutherland, G.; Antalis, T.
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.
1995Assignment of the human skeletal muscle a-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridizationEyre, H.; Akkari, P.; Wilton, S.; Callen, D.; Baker, E.; Laing, N.
1995The human OTF1 locus which overlaps the CD3Z gene is located at 1q22>q23Sturm, R.; Eyre, H.; Baker, E.; Sutherland, G.
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.
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.
1998Construction of a high-resolution physical and transcription map of chromosome 16q24.3 - a region of frequent loss of heterozygosity in sporadic breast cancerWhitmore, S.; Crawford, J.; Apostolou, S.; Eyre, H.; Baker, E.; Lower, K.; Settasatian, C.; Goldup, S.; Seshadri, R.; Gibson, R.; Mathew, C.; Cleton-Jansen, A.M.; Savoia, A.; Pronk, J.; Auerbach, A.; Doggett, N.; Sutherland, G.; Callen, D.

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