Nucleic Acid Amplification Strategies for Diagnosis of Heritable Diseases
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Publisher
Birkhäuser Boston
Link
http://link.springer.com/content/pdf/10.1007/978-1-4612-2454-9_18.pdf
Reference135 articles.
1. Akli, S., J. Chelly, J.M. Lacorte, L. Poenaru and A. Kahn. 1991. Seven novel Tay-Sachs mutations detected by chemical mismatch cleavage of PCR-amplified cDNA fragments. Genomics 11:124–134.
2. al-Mahdawi, S., S. Chamberlain, L. Chojnowksa, E. Michalak, P. Nihoyannopoulos, M. Ryan, B. Kusnierczyk, J.A. French, D.M. Gilligan, J. Cleland, R. Williamson, W. Ruzyllo and C. Oakley. 1994. The electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 gene. Br. Heart J. 72:105–111.
3. Andersen, T.I. and A.L. Borresen. 1995. Alterations of the TP53 gene as a potential prognostic marker in breast carcinomas: advantages of using constant denaturant gel-electrophoresis in mutation detection. Diagn. Mol. Pathol. 4:203–211.
4. Aslanidis, C., G. Jansen, C. Amemiya, G. Shutler, M. Mahadevan, C. Tsilfidis, C. Chen, J. Alleman, N.G.M. Wormskamp, M. Vooijs, J. Buxton, K. Johnson, H J.M. Smeets, G.G. Lenon, A. Carrano, R.G. Korneluk, B. Wieringa and P.J. de Jong. 1992. Cloning of the essential myotonic dystrophy region and mapping of the putative defect. Nature 355:548–551.
5. Barany, F.1991. Genetic disease detection and DNA amplification using cloned thermostable ligase. Proc. Natl. Acad. Sci. USA 88:189–193.
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