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Results 1-10 of 14 (Search time: 0.008 seconds).
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PreviewIssue DateTitleAuthor(s)
1997Dynamic mutation: possible mechanisms and significance in human diseaseRichards, R.; Sutherland, G.
1997Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeatYu, S.; Mangelsdorf, M.; Hewett, D.; Hobson, L.; Baker, E.; Eyre, H.; Lapsys, N.; Le Paslier, D.; Doggett, N.; Sutherland, G.; Richards, R.
1997FMR2 expression in families with FRAXE mental retardationGecz, J.; Oostra, B.; Hockey, A.; Carbonell, P.; Turner, G.; Haan, E.; Sutherland, G.; Mulley, J.
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.
1997Gene structure and subcellular localisation of FMR2, a member of a new family of putative transcription activatorsGecz, J.; Bielby, S.; Sutherland, G.; Mulley, J.
1997Localisation of a 10q breakpoint within the PAX2 gene in a patient with a de novo t(10;13) translocation and optic nerve coloboma-renal diseaseNarahara, K.; Baker, E.; Ito, S.; Yokoyama, Y.; Yu, S.; Hewitt, D.; Sutherland, G.; Eccles, M.; Richards, R.
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.
1997Cloning, characterisation and chromosomal assignment of the human adenosine A3 receptor (ADORA3) geneAtkinson, M.; Townsend-Nicholson, A.; Nicholl, J.; Sutherland, G.; Schofield, P.
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.
1997Mapping of the gene for vascular endothelial growth factor-D in mouse and man to the X chromosomeJenkins, N.; Woollatt, E.; Crawford, J.; Gilbert, D.; Baldwin, M.; Sutherland, G.; Copeland, N.; Achen, M.