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Human Mutation|April 24, 2001
Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancersS M Lipkin, V Wang, D L Stoler, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1988
Chromosome jumping from D4S10 (G8) toward the Huntington disease geneJ E Richards, T C Gilliam, J L Cole, et al.Blood|December 1, 1984
Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black populationF S Collins, C D Boehm, P G Waber, et al.The American Journal of Physiology|July 1, 1997
CFTR activation: additive effects of stimulatory and inhibitory phosphorylation sites in the R domainD J Wilkinson, T V Strong, M K Mansoura, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 1989
Identification of the structural mutation responsible for the dibucaine-resistant (atypical) variant form of human serum cholinesteraseM C McGuire, C P Nogueira, C F Bartels, et al.Somatic Cell and Molecular Genetics|May 1, 1993
Neurofibromatosis type 1 gene product (neurofibromin) associates with microtubulesP E Gregory, D H Gutmann, A Mitchell, et al.Nucleic Acids Research|January 25, 1990
Approaches to localizing disease genes as applied to cystic fibrosisM Dean, M L Drumm, C Stewart, et al.Annals of the New York Academy of Sciences|January 1, 1990
Expression of human globin genes in transgenic mice carrying the beta-globin gene cluster with a mutation causing G gamma beta + hereditary persistence of fetal hemoglobinM Tanaka, J A Nolan, A K Bhargava, et al.Nature Genetics|February 14, 1998
Evolutionary sequence comparisons using high-density oligonucleotide arraysJ G Hacia, W Makalowski, K Edgemon, et al.Genome Research|January 5, 1999
Strategies for mutational analysis of the large multiexon ATM gene using high-density oligonucleotide arraysJ G Hacia, B Sun, N Hunt, et al.Pageof 24