D N Cooper

发表

The human gene mutation database

M Krawczak, D. Cooper, M. Krawczak, 1998, Nucleic Acids Res..

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition.

E G Tuddenham, S. Antonarakis, D. Cooper, 1994, Nucleic acids research.

Human Gene Mutation Database: towards a comprehensive central mutation database

P. Stenson, D. Cooper, M. Mort, 2007, Journal of Medical Genetics.

Factor VIII gene inversions in severe hemophilia A: results of an international consortium study.

F E Preston, P G Mori, S S Sommer, 1995, Blood.

Single base‐pair substitutions in pathology and evolution: Two sides to the same coin

M Krawczak, D. Cooper, M. Krawczak, 1996, Human mutation.

Unmethylated domains in vertebrate DNA.

A. Bird, D. Cooper, M. Taggart, 1983, Nucleic acids research.

Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions

D. Cooper, J. Högel, H. Kehrer-Sawatzki, 2010, Journal of Medical Genetics.

The effect of replication errors on the mismatch analysis of PCR-amplified DNA.

M Krawczak, D. Cooper, M. Krawczak, 1990, Nucleic acids research.

Mosaicism in sporadic neurofibromatosis type 1: variations on a theme common to other hereditary cancer syndromes?

D. Cooper, H. Kehrer-Sawatzki, D N Cooper, 2008, Journal of Medical Genetics.

Estimating the efficacy and efficiency of cascade genetic screening.

M Krawczak, D. Cooper, M. Krawczak, 2001, American journal of human genetics.

Somatic spectrum of cancer‐associated single basepair substitutions in the TP53 gene is determined mainly by endogenous mechanisms of mutation and by selection

M Krawczak, E. Hovig, D. Cooper, 1995, Human mutation.

Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes.

M Krawczak, D. Cooper, M. Krawczak, 1998, American journal of human genetics.