| Literature DB >> 8353415 |
Abstract
The use of simple sequence repeats as polymorphic genetic markers has significantly facilitated the construction of reference maps of the human chromosomes and the mapping of mendelian genetic diseases. These markers display major advantages over other systems, including restriction fragment length polymorphisms and satellites, but also have some limitations.Entities:
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Year: 1993 PMID: 8353415 DOI: 10.1016/0959-437x(93)90114-5
Source DB: PubMed Journal: Curr Opin Genet Dev ISSN: 0959-437X Impact factor: 5.578