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Clinical Chemistry 43: 1114-1128, 1997;
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(Clinical Chemistry. 1997;43:1114-1128.)
© 1997 American Association for Clinical Chemistry, Inc.


Review

Methods for detection of point mutations: performance and quality assessment

Peter Nollau, Christoph Wagenera, on behalf of the IFCC Scientific Division and Committee on Molecular Biology Techniques

Department of Clinical Chemistry, Medical Clinic, University Hospital Eppendorf, Martinistr. 52, D-20251 Hamburg, Germany.
a Author for correspondence. Fax +494047174621; e-mail wagener{at}uke.uni-hamburg.de

We give an overview of current methods for the detection of point mutations as well as small insertions and deletions in clinical diagnostics. For each method, the following characteristics are specified: (a) principle, (b) major modifications, (c) maximum fragment size that can be analyzed, (d) ratio and type of mutations that can be detected, (e) minimum ratio of mutant to wild-type alleles at which mutations can be detected, and (f) detection methods. Special attention is paid to the possibilities of quality assessment and the potential for standardization and automation.


Key Words: indexing terms: alleles • electrophoresis • gene insertions • gene deletions • polymerase chain reaction




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