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Results 51-60 of 83 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
1995Molecular cloning of the cDNA encoding human skeletal muscle triadin and its localisation to chromosome 6q22-6q23Taske, N.; Eyre, H.; O'Brien, R.; Sutherland, G.; Denborough, M.; Foster, P.
1995Natural killer cell receptor for HLA-B allotypes, NKB1 map position 19q13.4Baker, E.; D'Andrea, A.; Phillips, J.; Sutherland, G.; Lanier, L.
1995Assignment of the human pyruvate carboxylase gene (PC) to 11q13.4 by fluorescence in situ hybridisationWalker, M.; Baker, E.; Wallace, J.; Sutherland, G.
1999Partial seizures with focal epileptogenic electroencephalographic patterns in three related female patients with fragile-X syndromeSingh, R.; Sutherland, G.; Manson, J.
1997Cloning, characterisation and chromosomal assignment of the human adenosine A3 receptor (ADORA3) geneAtkinson, M.; Townsend-Nicholson, A.; Nicholl, J.; Sutherland, G.; Schofield, P.
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.
1996Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21Wallace, R.; Berkovic, S.; Howell, R.; Sutherland, G.; Mulley, J.
1996FRAGILE X SYNDROME AND FRAGILE XE MENTAL RETARDATION [Review]Sutherland, G.; Mulley, J.
1995A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsySteinlein, O.; Mulley, J.; Propping, P.; Wallace, R.; Phillips, H.; Sutherland, G.; Scheffer, I.; Berkovic, S.
1995The human OTF1 locus which overlaps the CD3Z gene is located at 1q22>q23Sturm, R.; Eyre, H.; Baker, E.; Sutherland, G.