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PreviewIssue DateTitleAuthor(s)
2001Isolation, tissue distribution, and chromosomal localization of a novel testis-specific human four-transmembrane gene related to CD20 and FcRI-bHulett, M.; Pagler, E.; Hornby, J.; Hogarth, P.; Eyre, H.; Baker, E.; Crawford, J.; Sutherland, G.; Ohms, S.; Parish, C.
2002Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomaliesBaker, E.; Hinton, L.; Callen, D.; Altree, M.; Dobbie, A.; Eyre, H.; Sutherland, G.; Thompson, E.; Thompson, P.; Woollatt, E.; Haan, E.
2005Frequency of truly cryptic subtelomere abnormalities - a study of 534 patients and literature reviewYu, S.; Baker, E.; Hinton, L.; Eyre, H.; Waters, W.; Higgins, S.; Sutherland, G.; Haan, E.
1999Gamma-Heregulin: a fusion gene of DOC-4 and neuregulin-1 derived from a chromosome translocationLiu, X.; Baker, E.; Eyre, H.; Sutherland, G.; Zhou, M.
1998FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesisHewett, D.; Handt, O.; Hobson, L.; Mangelsdorf, M.; Eyre, H.; Baker, E.; Sutherland, G.; Schuffenhauer, S.; Mao, J.; Richards, R.
1995The human OTF1 locus which overlaps the CD3Z gene is located at 1q22>q23Sturm, R.; Eyre, H.; Baker, E.; 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.
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.