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Electrophoresis. 1996 Jan;17(1):247-54.

Genetic screening and testing by induced heteroduplex formation.

Author information

1
Department of Transplantation Sciences, University of Bristol, UK.

Abstract

Clustered point mutations and small deletions or insertions within DNA are amenable to rapid analysis using induced heteroduplex formation. A single synthetic molecule (universal heteroduplex generator, UHG) may detect any of a series of such mutations following amplification by the polymerase chain reaction. This paper illustrates the use of UHG-based DNA heteroduplex analysis by describing the construction, properties, and methods of use of five UHGs, designed for genetic screening and testing of the inherited metabolic diseases: phenylketonuria, sickle-cell disease, cystic fibrosis, von Willebrand's disease type 2B, and mamman-binding lectin deficiency. In all cases, identification of multiple disease-associated genotypes is possible using a single UHG.

PMID:
8907549
DOI:
10.1002/elps.1150170143
[Indexed for MEDLINE]

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