Authors:
Wiltshire, S
Hattersley, AT
Hitman, GA
Walker, M
Levy, JC
Sampson, M
O'Rahilly, S
Frayling, TM
Bell, JI
Lathrop, GM
Bennett, A
Dhillon, R
Fletcher, C
Groves, CJ
Jones, E
Prestwich, P
Simecek, N
Rao, PVS
Wishart, M
Foxon, R
Howell, S
Smedley, D
Cardon, LR
Menzel, S
McCarthy, MI
Citation: S. Wiltshire et al., A genomewide scan for loci predisposing to type 2 diabetes in a UK population (the Diabetes UK Warren 2 repository): Analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q, AM J HU GEN, 69(3), 2001, pp. 553-569
Authors:
Sorour, A
Brito-Babapulle, V
Smedley, D
Yuille, M
Catovsky, D
Citation: A. Sorour et al., Unusual breakpoint distribution of 8p abnormalities in T-prolymphocytic leukemia: A study with YACS mapping to 8p11-p12, CANC GENET, 121(2), 2000, pp. 128-132
Authors:
Kulkarni, S
Reiter, A
Smedley, D
Goldman, JM
Cross, NCP
Citation: S. Kulkarni et al., The genomic structure of ZNF198 and location of breakpoints in the t(8;13)myeloproliferative syndrome, GENOMICS, 55(1), 1999, pp. 118-121
Authors:
Lu, YJ
Birdsall, S
Summersgill, B
Smedley, D
Osin, P
Fisher, C
Shipley, J
Citation: Yj. Lu et al., Dual colour fluorescence in-situ hybridization to paraffin-embedded samples to deduce the presence of the der(X)t(X;18)(p11.2;q11.2) and involvement of either the SSX1 or SSX2 gene: A diagnostic and prognostic aid for synovial sarcoma, J PATHOLOGY, 187(4), 1999, pp. 490-496