Authors: Lloyd, SE Onwuazor, ON Beck, JA Mallinson, G Farrall, M Targonski, P Collinge, J Fisher, EMC

Citation: Se. Lloyd et al., Identification of multiple quantitative trait loci linked to prion diseaseincubation period in mice, P NAS US, 98(11), 2001, pp. 6279-6283

Authors: Scheinman, SJ Cox, JPD Lloyd, SE Pearce, SHS Salenger, PV Hoopes, RR Bushinsky, DA Wrong, O Asplin, JR Langman, CB Norden, AGW Thakker, RV

Citation: Sj. Scheinman et al., Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria, KIDNEY INT, 57(1), 2000, pp. 232-239

Authors: Bosio, M Bianchi, ML Lloyd, SE Thakker, RV

Citation: M. Bosio et al., A familial syndrome due to Arg648Stop mutation in the X-linked renal chloride channel gene, PED NEPHROL, 13(4), 1999, pp. 278-283

Authors: Lloyd, SE Pannett, AAJ Dixon, PH Whyte, MP Thakker, RV

Citation: Se. Lloyd et al., Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13, AM J HU GEN, 64(1), 1999, pp. 189-195