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Results 1-10 of 21 (Search time: 0.005 seconds).
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PreviewIssue DateTitleAuthor(s)
1996Fragile X Syndrome and other X-linked Causes of Mental HandicapSutherland, G.; Mulley, J.
1996Identification of the gene FMR2, associated with FRAXE mental retardationGecz, J.; Gedeon, A.; Sutherland, G.; Mulley, J.
1996FRAGILE X SYNDROME AND FRAGILE XE MENTAL RETARDATION [Review]Sutherland, G.; Mulley, J.
1996Positional cloning of the Fanconi anaemia group A geneApostolou, S.; Whitmore, S.; Crawford, J.; Lennon, G.; Sutherland, G.; Callen, D.; Ianzano, L.; Savino, M.; d'Apolito, M.; Notarangelo, A.; Memeo, E.; Piemontese, M.; Zelante, L.; Savoia, A.; Gibson, R.; Tipping, A.; Morgan, N.; Hassock, S.; Jansen, S.; de Ravel, T.; et al.
1996bcl-w, a novel member of the bcl-2 family, promotes cell survivalGibson, L.; Holmgreen, S.; Huang, D.; Bernand, O.; Copeland, N.; Jenkins, N.; Sutherland, G.; Baker, E.; Adams, J.; Cory, S.
1996REPEAT OFFENDERS - SIMPLE REPEAT SEQUENCES AND COMPLEX GENETIC PROBLEMS [Review]Richards, R.; Sutherland, G.
1996Molecular Characterization of a Nonneuronal Human Unc18 HomologZiegler, S.; Mortrud, M.; Swartz, A.; Baker, E.; Sutherland, G.; Burmeister, M.; Mulligan, J.
1996Isolation and characterization of cDNA clones for Humly9: the human homologue of mouse Ly9Sandrin, M.; Henning, M.; Lo, M.; Baker, E.; Sutherland, G.; McKenzie, I.
1996Assignment of the Human GRB14 Gene to Chromosome 2q22-q24 By Fluorescence in Situ HybridizationBaker, E.; Sutherland, G.; Sutherland, R.; Daly, R.
1996Chromosomal mapping of the gene (INPP5A) encoding the 43-kDa membrane-associated inositol polyphosphate 5-phosphatase to 10q26.3 by fluorescence in situ hybridizationMitchell, C.; Speed, C.; Nicholl, J.; Sutherland, G.