Mapping of the mouse homologue of the Wilson disease gene to mouse chromosome 8. by Reed, V, Williamson, P, Bull, P, Cox, D, Boyd, Y

FURTHER-STUDIES ON CONSERVED LOCI IN XP11.22-]P11.21 by Boyd, Y, Blair, H, Maslen, G, Reed, V, Uwechue, I, Rider, S, Monaco, A, Laval, S

Analysis of Mnk, the murine homologue of the locus for Menkes disease, in normal and mottled (Mo) mice. by George, A, Reed, V, Glenister, P, Chelly, J, Tümer, Z, Horn, N, Monaco, A, Boyd, Y

A 2-Mb YAC contig encompassing three loci (DXF34, DXS14, and DXS390) that lie between Xp11.2 translocation breakpoints associated with incontinentia pigmenti type 1. by Reed, V, Rider, S, Maslen, G, Hatchwell, E, Blair, H, Uwechue, I, Craig, I, Laval, S, Monaco, A, Boyd, Y

ANALYSIS OF MUTATIONS AT THE MOTTLED LOCUS IN THE MOUSE, THE POSTULATED MURINE HOMOLOG OF MENKE SYNDROME by Reed, V, George, A, Glenister, P, Chelly, J, Monaco, A, Tumer, Z, Horn, N, Cattanach, B, Lyon, M, Boyd, Y