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Results 1-10 of 96 (Search time: 0.004 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.
1997Dynamic mutation: possible mechanisms and significance in human diseaseRichards, R.; 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.
1996Identification of the gene FMR2, associated with FRAXE mental retardationGecz, J.; Gedeon, A.; Sutherland, G.; Mulley, J.
1999Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patientGecz, J.; Baker, E.; Donnelly, A.; Ming, J.; McDonald-McGinn, D.; Spinner, N.; Zackai, E.; 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.
1999C160rf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brainBhalla, K.; Eyre, H.; Whitmore, S.; Sutherland, G.; Callen, D.