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Results 1-10 of 15 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1995Fragile X syndrome and other dynamic mutation diseasesSutherland, G.; Richards, R.
1995Paracentric inversions do not normally generate monocentric recombinant chromosomesSutherland, G.; Callen, D.; McKinlay Gardner, R.
1995The closely linked genes encoding the myeloid nuclear differentation antigen (MNDA) and IFI16 exhibit contrasting haemopoietic expressionDawson, M.; Trapani, J.; Briggs, R.; Nicholl, J.; Sutherland, G.; Baker, E.
1995Assignment of the human neuropeptide Y gene to chromosome 7p15.1 by nonisotopic in situ hybridizationBaker, E.; Hort, Y.; Ball, H.; Sutherland, G.; Shine, J.; Herzog, H.
1995Localisation of the adenosine A2b receptor subtype (ADORA2B) to chromosome 17p11.2-p12 by FISH and PCR screening of somatic cell hybridsTownsend-Nicholson, A.; Baker, E.; Sutherland, G.; Schofield, P.
1995Chromosomal mapping of the human proteinase inhibitor 6 (PI6) gene to 6p25 by fluorescence in situ hybridizationCoughlin, P.; Nicholl, J.; Sun, J.; Salem, H.; Bird, P.; Sutherland, G.
1995Localisation of the adenosine A1 receptor subtype gene (ADORA1) to chromosome 1q32.1Townsend-Nicholson, A.; Baker, E.; Schofield, P.; Sutherland, G.
1995The CEPH consortium linkage map of human chromosome 16Kozman, H.; Keith, T.; Donis-Keller, H.; White, R.; Weissenbach, J.; Sutherland, G.
1995Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locusNancarrow, J.; Holman, K.; Hori, T.; Denton, M.; Sutherland, G.; Richards, R.
1995Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to 20q13.2Phillips, H.; Scheffer, I.; Berkovic, S.; Hollway, G.; Sutherland, G.; Mulley, J.