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Results 1-10 of 83 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1995Simple tandem DNA repeats and human genetic diseaseSutherland, G.; Richards, R.
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.
1995Molecular dissection of a contiguous gene syndrome: Localization of the genes involved in the Langer-Giedion syndromeLudecke, H.; Wagner, M.; Nardmann, J.; La Pillo, B.; Parrish, J.; Willems, P.; Sutherland, G.
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.
1996Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21Wallace, R.; Berkovic, S.; Howell, R.; Sutherland, G.; Mulley, J.
1999C160rf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brainBhalla, K.; Eyre, H.; Whitmore, S.; Sutherland, G.; Callen, D.
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.
1997FMR2 expression in families with FRAXE mental retardationGecz, J.; Oostra, B.; Hockey, A.; Carbonell, P.; Turner, G.; Haan, E.; Sutherland, G.; Mulley, J.
1995The CEPH consortium linkage map of human chromosome 16Kozman, H.; Keith, T.; Donis-Keller, H.; White, R.; Weissenbach, J.; Sutherland, G.