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Human Genetics|June 1, 1990
The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictionsD N Cooper, M KrawczakHuman Mutation|January 1, 1996
Single base-pair substitutions in pathology and evolution: two sides to the same coinM Krawczak, D N CooperHuman Genetics|September 1, 1989
Cytosine methylation and the fate of CpG dinucleotides in vertebrate genomesD N Cooper, M KrawczakHuman Genetics|March 1, 1991
Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environmentM Krawczak, D N CooperHuman Genetics|August 1, 1991
Mechanisms of insertional mutagenesis in human genes causing genetic diseaseD N Cooper, M KrawczakHuman Genetics|September 1, 1992
The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequencesM Krawczak, J Reiss, D N CooperAmerican Journal of Human Genetics|June 30, 2001
Estimating the efficacy and efficiency of cascade genetic screeningM Krawczak, D N Cooper, J SchmidtkeHuman Genetics|September 1, 1996
Molecular reconstruction and homology modelling of the catalytic domain of the common ancestor of the haemostatic vitamin-K-dependent serine proteinasesM Krawczak, A Wacey, D N CooperAmerican Journal of Human Genetics|July 31, 1998
Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genesM Krawczak, E V Ball, D N CooperEuropean Journal of Pediatrics|February 24, 2001
Disease-causing mutations in the human genomeS E Antonarakis, M Krawczak, D N CooperPageof 26