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Preview	Issue Date	Title	Author(s)
	1995	The brn-2 gene regulates the melanocytic phenotype and tumorigenic potential of human melanoma cells	Angus, J.; Thompson, F.; Murphy, K.; Baker, E.; Sutherland, G.; Parsons, P.; Sturm, R.
	2000	The clinical significance of fragile sites on human chromosomes	Sutherland, G.; Baker, E.
	1995	The closely linked genes encoding the myeloid nuclear differentation antigen (MNDA) and IFI16 exhibit contrasting haemopoietic expression	Dawson, M.; Trapani, J.; Briggs, R.; Nicholl, J.; Sutherland, G.; Baker, E.
	1995	The genes encoding the myeloid nuclear differentiation antigen (MNDA) and IFI 16 are closely linked on human chromosome 1q22 but exhibit contrasting expression in haemopoietic cell lnes	Dawson, M.; Trapani, J.; Briggs, R.; Nicholl, J.; Sutherland, G.; Baker, E.
	1996	The human glycine receptor β subunit: primary structure, functional characterisation and chromosomal localisation of the human and murine genes	Handford, C.; Lynch, J.; Baker, E.; Webb, G.; Ford, J.; Sutherland, G.; Schofield, P.
	1995	The human OTF1 locus which overlaps the CD3Z gene is located at 1q22>q23	Sturm, R.; Eyre, H.; Baker, E.; Sutherland, G.
	2005	The Hunter-McAlpine syndrome results from duplication 5q35-qter	Hunter, A.; DuPont, B.; McLaughlin, M.; Hinton, L.; Baker, E.; Ades, L.; Haan, E.; Schwartz, C.
	2010	The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletion	MacKinnon, R.; Selan, C.; Wall, M.; Baker, E.; Nandurkar, H.; Campbell, L.
	2003	Transfer of chromosome 8 into two breast cancer cell lines: total exclusion of three regions indicates location of putative in vitro growth suppressor genes	Wilson, P.; Cuthbert, A.; Marsh, A.; Arnold, J.; Flanagan, J.; Mulford, C.; Trott, D.; Baker, E.; Purdie, D.; Newbold, R.; Chenevix-Trench, G.
	2003	Two further cases of Ohdo syndrome delineate the phenotypic variability of the condition	White, S.; Ades, L.; Amor, D.; Liebelt, J.; Bankier, A.; Baker, E.; Wilson, M.; Savarirayan, R.
	1997	Unbalanced t(4;11)(q32-q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromes	Byatt, S.; Baker, E.; Richards, R.; Roberts, C.; Smith, A.

Showing results 42 to 52 of 52 < previous