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Results 1-10 of 32 (Search time: 0.009 seconds).
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PreviewIssue DateTitleAuthor(s)
1995Simple tandem DNA repeats and human genetic diseaseSutherland, G.; Richards, R.
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.
1995The CEPH consortium linkage map of human chromosome 16Kozman, H.; Keith, T.; Donis-Keller, H.; White, R.; Weissenbach, J.; Sutherland, G.
1995The molecular basis of fragile sites in human chromosomesSutherland, G.; Richards, R.
1995Natural killer cell receptor for HLA-B allotypes, NKB1 map position 19q13.4Baker, E.; D'Andrea, A.; Phillips, J.; Sutherland, G.; Lanier, L.
1995Paracentric inversions do not normally generate monocentric recombinant chromosomesSutherland, G.; Callen, D.; McKinlay Gardner, R.
1995Overlapping submicroscopic deletions in Xq28 causing developmental disorders in two unrelated boysGedeon, A.; Keinanen, M.; Ades, L.; Kaarianen, H.; Gecz, J.; Baker, E.; Sutherland, G.; Mulley, J.
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.