Abstract
Full text
PDF
Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Danenberg P. V., Horikoshi T., Volkenandt M., Danenberg K., Lenz H. J., Shea L. C., Dicker A. P., Simoneau A., Jones P. A., Bertino J. R. Detection of point mutations in human DNA by analysis of RNA conformation polymorphism(s). Nucleic Acids Res. 1992 Feb 11;20(3):573–579. doi: 10.1093/nar/20.3.573. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lázaro C., Estivill X. Mutation analysis of genetic diseases by asymmetric-PCR SSCP and ethidium bromide staining: application to neurofibromatosis and cystic fibrosis. Mol Cell Probes. 1992 Oct;6(5):357–359. doi: 10.1016/0890-8508(92)90027-u. [DOI] [PubMed] [Google Scholar]
- Orita M., Iwahana H., Kanazawa H., Hayashi K., Sekiya T. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. Proc Natl Acad Sci U S A. 1989 Apr;86(8):2766–2770. doi: 10.1073/pnas.86.8.2766. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sarkar G., Yoon H. S., Sommer S. S. Screening for mutations by RNA single-strand conformation polymorphism (rSSCP): comparison with DNA-SSCP. Nucleic Acids Res. 1992 Feb 25;20(4):871–878. doi: 10.1093/nar/20.4.871. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Spinardi L., Mazars R., Theillet C. Protocols for an improved detection of point mutations by SSCP. Nucleic Acids Res. 1991 Jul 25;19(14):4009–4009. doi: 10.1093/nar/19.14.4009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- White M. B., Carvalho M., Derse D., O'Brien S. J., Dean M. Detecting single base substitutions as heteroduplex polymorphisms. Genomics. 1992 Feb;12(2):301–306. doi: 10.1016/0888-7543(92)90377-5. [DOI] [PubMed] [Google Scholar]