Resolving DNA mutations
- 1 February 1995
- journal article
- Published by Springer Nature in Nature Genetics
- Vol. 9 (2) , 103-104
- https://doi.org/10.1038/ng0295-103
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Detection of mutations by cleavage of DNA heteroduplexes with bacteriophage resolvasesNature Genetics, 1995
- Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII.Proceedings of the National Academy of Sciences, 1995
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994
- Optimization of the single-strand conformation polymorphism (SSCP) technique for detection of point mutationsHuman Mutation, 1993
- Detecting single base substitutions as heteroduplex polymorphismsGenomics, 1992
- DNA sequence polymorphisms in Alu repeatsGenomics, 1990
- Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes.Proceedings of the National Academy of Sciences, 1989
- Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations.Proceedings of the National Academy of Sciences, 1988
- Detection of Single Base Substitutions by Ribonuclease Cleavage at Mismatches in RNA:DNA DuplexesScience, 1985
- Detection of single base substitutions in total genomic DNANature, 1985