| P2093 | author name string | Mike Makrigiorgos G | |
| P2860 | cites work | Laser capture microdissection | Q28293867 |
| | Linkage disequilibrium in the human genome | Q29616097 |
| | Detection of simple mutations and polymorphisms in large genomic regions | Q30715152 |
| | Tech.Sight. Understanding disease cell by cell. | Q31057519 |
| | The mutY gene: a mutator locus in Escherichia coli that generates G.C----T.A transversions | Q33567384 |
| | Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations | Q33582011 |
| | A sensitive scanning technology for low frequency nuclear point mutations in human genomic DNA. | Q33631409 |
| | Enzymatic and chemical cleavage methods | Q33669200 |
| | Quantitative detection of single nucleotide polymorphisms for a pooled sample by a bioluminometric assay coupled with modified primer extension reactions (BAMPER) | Q33948446 |
| | Haplotype variation and linkage disequilibrium in 313 human genes | Q33953585 |
| | Fidelity of DNA polymerases in DNA amplification | Q34322626 |
| | A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies | Q34385302 |
| | Prospects for applying genotypic selection of somatic oncomutation to chemical risk assessment | Q34416553 |
| | Genomic sequencing and methylation analysis by ligation mediated PCR. | Q34550393 |
| | Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII. | Q34804051 |
| | Association mapping of disease loci, by use of a pooled DNA genomic screen | Q35249321 |
| | Effects of different DNA polymerases in ligation-mediated PCR: enhanced genomic sequencing and in vivo footprinting | Q36815765 |
| | Ligation of a primer at a mutation: a method to detect low level mutations in DNA. | Q38363467 |
| | An amplification and ligation-based method to scan for unknown mutations in DNA. | Q38364134 |
| | Detecting colorectal cancer in stool with the use of multiple genetic targets | Q39569642 |
| | Rapid detection of the factor V Leiden (1691 G > A) and haemochromatosis (845 G > A) mutation by fluorescence resonance energy transfer (FRET) and real time PCR. | Q39621691 |
| | Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutations | Q39723322 |
| | Mutation detection using a novel plant endonuclease | Q39725311 |
| | Novel amplification of DNA in a hairpin structure: towards a radical elimination of PCR errors from amplified DNA. | Q39744781 |
| | Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers | Q40538213 |
| | Mutational spectrometry: means and ends. | Q40597365 |
| | A versatile mismatch recognition agent: specific cleavage of a plasmid DNA at a single base mispair | Q41645389 |
| | Genotypic selection methods for the direct analysis of point mutations | Q41645720 |
| | A simple and accurate method for determination of microsatellite total allele content differences between DNA pools | Q41727943 |
| | Mapping of copper/hydrogen peroxide-induced DNA damage at nucleotide resolution in human genomic DNA by ligation-mediated polymerase chain reaction | Q43769111 |
| | Sensitive and quantitative detection of mutations associated with clinical resistance to STI-571. | Q44512456 |
| | Truncated amplification: a method for high-fidelity template-driven nucleic acid amplification | Q47569168 |
| | Detection of hotspot mutations and polymorphisms using an enhanced PCR-RFLP approach | Q47995789 |
| | Needle-in-a-haystack detection and identification of base substitution mutations in human tissues. | Q53419192 |
| | Substrate specificity of Escherichia coli MutY protein. | Q54579279 |
| | Detection of single base substitutions in total genomic DNA | Q59092301 |
| | Large-scale genotyping of single nucleotide polymorphisms by Pyrosequencing? and validation against the 5?nuclease (Taqman�) assay | Q63502685 |
| | MutY DNA glycosylase: base release and intermediate complex formation | Q64389057 |
| | Ligation of single-stranded oligodeoxyribonucleotides by T4 RNA ligase | Q69711519 |
| | Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders | Q73911223 |
| | Assessing allele frequencies of single nucleotide polymorphisms in DNA pools by pyrosequencing technology | Q74133504 |
| | Mutation detection using fluorescent enzyme mismatch cleavage with T4 endonuclease VII | Q77918358 |
| P433 | issue | 5 | |
| P304 | page(s) | 406-412 | |
| P577 | publication date | 2004-05-01 | |
| P1433 | published in | Human Mutation | Q5937269 |
| P1476 | title | PCR-based detection of minority point mutations | |
| P478 | volume | 23 | |