Items where Author is "Ball, EV"

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Journal article

COOPER, D.N., CHEN, J.M., BALL, E.V., HOWELLS, K., MORT, M., PHILLIPS, A.D., CHUZHANOVA, N., KEHRER-SAWATZKI, H. and STEPHENS, M., 2010. Genes, mutations and human inherited disease at the dawn of the 100K mutome era. Human Mutation, 31, pp. 631-655.

COOPER, D.N., MORT, M., STENSON, P.D., BALL, E.V. and CHUZHANOVA, N.A., 2010. Methylation-mediated deamination of 5-methylcytosine appears to give rise to mutations causing human inherited disease in CpNpG trinucleotides as well as in CpG dinucleotides. Human Genomics, 4, pp. 406-410.

BALL, E.V., STENSON, P.D., KRAWCZAK, M., COOPER, D.N. and CHUZHANOVA, N., 2005. Micro-deletions and micro-insertions causing human genetic disease: common mechanisms of mutagenesis and the role of local DNA sequence complexity. Human Mutation, 26, pp. 205-213.

ABEYSINGHE, S.S., CHUZHANOVA, N., KRAWCZAK, M., BALL, E.V. and COOPER, D.N., 2003. Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs. Human Mutation, 22 (3), pp. 229-244.

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