Showing results (21-30 of 255) with videos related to
Sort By:
Pageof 26
Human Genetics|August 1, 1991
Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) geneJ Reiss, D N Cooper, J Bal, et al.Gene|September 7, 2000
Promoter shuffling has occurred during the evolution of the vertebrate growth hormone geneN A Chuzhanova, M Krawczak, L A Nemytikova, et al.Human Genetics|March 1, 1992
Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C geneC B Grundy, S Schulman, M Krawczak, et al.Human Mutation|January 1, 1995
Somatic spectrum of cancer-associated single basepair substitutions in the TP53 gene is determined mainly by endogenous mechanisms of mutation and by selectionM Krawczak, B Smith-Sorensen, J Schmidtke, et al.Human Genetics|January 1, 1985
Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IXB Zoll, J Arnemann, M Krawczak, et al.Human Genetics|December 29, 2000
Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regionsM Krawczak, N A Chuzhanova, P D Stenson, et al.Human Mutation|December 29, 1999
Human gene mutation database-a biomedical information and research resourceM Krawczak, E V Ball, I Fenton, et al.Human Genetics|January 26, 2002
ASP--a simulation-based power calculator for genetic linkage studies of qualitative traits, using sib-pairsM KrawczakElectrophoresis|February 1, 1994
Multilocus DNA fingerprinting: the independence problem in quantitative paternity testingM KrawczakHuman Genetics|February 1, 1987
Genetic risk and recombination fraction--an example of non-monotonic dependencyM KrawczakPageof 26