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Preview	Issue Date	Title	Author(s)
	2004	Tissue plasminogen activator-7351C/T enhancer polymorphism is a risk factor for lacunar stroke	Jannes, J.; Hamilton-Bruce, M.; Pilotto, L.; Smith, B.; Mullighan, C.; Bardy, P.; Koblar, S.
	2000	New mutations in MID1 provide support for loss of function as the cause of X-linked Optiz syndrome	Cox, T.; Allen, L.; Cox, L.; Hopwood, B.; Goodwin, B.; Haan, E.; Suthers, G.
	2007	Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation	Tarpey, P.; Raymond, F.; Nguyen, L.; Rodriguez, J.; Hackett, A.; Vandeleur, L.; Smith, R.; Shoubridge, C.; Edkins, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Hills, K.; Jones, D.; Mironenko, T.; Perry, J.; et al.
	2004	Analysis of intracranial volume in Apert Syndrome genotypes	Anderson, P.; Netherway, D.; Abbott, A.; Cox, T.; Roscioli, T.; David, D.
	2007	Array comparative genomic hybridisation analysis of boys with X-linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3	Solomon, N.; Ross, S.; Forrest, S.; Thomas, P.; Morgan, T.; Belsky, J.; Hol, F.; Karnes, P.; Hopwood, N.; Myers, S.; Tan, A.; Warne, G.
	2004	Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus	Dudding, T.; Friend, K.; Schofield, P.; Lee, S.; Wilkinson, I.; Richards, R.
	2002	Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c	Schwarz, Q.; Cox, T.