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Results 1-10 of 33 (Search time: 0.008 seconds).
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PreviewIssue DateTitleAuthor(s)
1996The human glycine receptor β subunit: primary structure, functional characterisation and chromosomal localisation of the human and murine genesHandford, C.; Lynch, J.; Baker, E.; Webb, G.; Ford, J.; Sutherland, G.; Schofield, P.
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.
1999Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patientGecz, J.; Baker, E.; Donnelly, A.; Ming, J.; McDonald-McGinn, D.; Spinner, N.; Zackai, E.; Sutherland, G.; Mulley, J.
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.
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.; Savoia, A.; Pronk, J.; Auerbach, A.; Doggett, N.; Sutherland, G.; Callen, D.
1996Assignment of the Gene For Beta-Casein (CSN2) to 4q13-q21 in Humans and 3p13-p12 in ChimpanzeesMcConkey, E.; Menon, R.; Williams, G.; Baker, E.; Sutherland, G.
1999Homozygotes for FRA16B are normalHocking, T.; Feichtinger, W.; Schmid, M.; Haan, E.; Baker, E.; Sutherland, G.
1995Natural killer cell receptor for HLA-B allotypes, NKB1 map position 19q13.4Baker, E.; D'Andrea, A.; Phillips, J.; Sutherland, G.; Lanier, L.
1998Fragile sites still breaking [Review]Sutherland, G.; Baker, E.; Richards, R.
1995Overlapping submicroscopic deletions in Xq28 causing developmental disorders in two unrelated boysGedeon, A.; Keinanen, M.; Ades, L.; Kaarianen, H.; Gecz, J.; Baker, E.; Sutherland, G.; Mulley, J.