| pubmed-article:1979162 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1979162 | lifeskim:mentions | umls-concept:C0012854 | lld:lifeskim |
| pubmed-article:1979162 | lifeskim:mentions | umls-concept:C0017393 | lld:lifeskim |
| pubmed-article:1979162 | lifeskim:mentions | umls-concept:C1264693 | lld:lifeskim |
| pubmed-article:1979162 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
| pubmed-article:1979162 | lifeskim:mentions | umls-concept:C0206415 | lld:lifeskim |
| pubmed-article:1979162 | pubmed:issue | 22 | lld:pubmed |
| pubmed-article:1979162 | pubmed:dateCreated | 1991-1-15 | lld:pubmed |
| pubmed-article:1979162 | pubmed:abstractText | Molecular genetic maps are commonly constructed by analyzing the segregation of restriction fragment length polymorphisms (RFLPs) among the progeny of a sexual cross. Here we describe a new DNA polymorphism assay based on the amplification of random DNA segments with single primers of arbitrary nucleotide sequence. These polymorphisms, simply detected as DNA segments which amplify from one parent but not the other, are inherited in a Mendelian fashion and can be used to construct genetic maps in a variety of species. We suggest that these polymorphisms be called RAPD markers, after Random Amplified Polymorphic DNA. | lld:pubmed |
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| pubmed-article:1979162 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1979162 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1979162 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1979162 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:1979162 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1979162 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1979162 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1979162 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:1979162 | pubmed:issn | 0305-1048 | lld:pubmed |
| pubmed-article:1979162 | pubmed:author | pubmed-author:WilliamsJ GJG | lld:pubmed |
| pubmed-article:1979162 | pubmed:author | pubmed-author:LivakK JKJ | lld:pubmed |
| pubmed-article:1979162 | pubmed:author | pubmed-author:RafalskiJ AJA | lld:pubmed |
| pubmed-article:1979162 | pubmed:author | pubmed-author:TingeyS VSV | lld:pubmed |
| pubmed-article:1979162 | pubmed:author | pubmed-author:KubelikA RAR | lld:pubmed |
| pubmed-article:1979162 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1979162 | pubmed:day | 25 | lld:pubmed |
| pubmed-article:1979162 | pubmed:volume | 18 | lld:pubmed |
| pubmed-article:1979162 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1979162 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1979162 | pubmed:pagination | 6531-5 | lld:pubmed |
| pubmed-article:1979162 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:1979162 | pubmed:year | 1990 | lld:pubmed |
| pubmed-article:1979162 | pubmed:articleTitle | DNA polymorphisms amplified by arbitrary primers are useful as genetic markers. | lld:pubmed |
| pubmed-article:1979162 | pubmed:affiliation | Central Research and Development Department, E.I. du Pont de Nemours & Co., Inc, Wilmington, DE 19880. | lld:pubmed |
| pubmed-article:1979162 | pubmed:publicationType | Journal Article | lld:pubmed |
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