Items where Author is "Wells, RD"

Journal article

CHUZHANOVA, N., CHEN, J.M., BACOLLA, A., PATRINOS, G.P., FEREC, C., WELLS, R.D. and COOPER, D.N., 2009. Gene conversion causing human inherited disease: evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair. Human Mutation, 30 (8), pp. 1189-1198. ISSN 1059-7794

BACOLLA, A., COLLINS, J.R., GOLD, B., CHUZHANOVA, N., YI, M., STEPHENS, R.M., STEFANOV, S., OLSH, A., JAKUPCIAK, J.P., DEAN, M., LEMPICKI, R.A., COOPER, D.N. and WELLS, R.D., 2006. Long homopurine•homopyrimidine sequences are characteristic of genes expressed in brain and the pseudoautosomal region. Nucleic Acids Research, 34, pp. 2663-2675.

BACOLLA, A., JAWORSKI, A., LARSON, J.E., JAKUPCIAK, J.P., CHUZHANOVA, N.A., ABEYSINGHE, S.S., O'CONNELL, C.D., COOPER, D.N. and WELLS, R.D., 2004. Breakpoints of gross deletions coincide with non-B DNA conformations. Proceedings of the National Academy of Sciences of the United Statesof America (PNAS), 101, pp. 14162-14167.