pubmed-article:1785656 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:1785656 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:1785656 | lifeskim:mentions | umls-concept:C1556094 | lld:lifeskim |
pubmed-article:1785656 | lifeskim:mentions | umls-concept:C0079259 | lld:lifeskim |
pubmed-article:1785656 | lifeskim:mentions | umls-concept:C0917713 | lld:lifeskim |
pubmed-article:1785656 | lifeskim:mentions | umls-concept:C0220908 | lld:lifeskim |
pubmed-article:1785656 | lifeskim:mentions | umls-concept:C0032520 | lld:lifeskim |
pubmed-article:1785656 | lifeskim:mentions | umls-concept:C0017260 | lld:lifeskim |
pubmed-article:1785656 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:1785656 | pubmed:dateCreated | 1992-3-18 | lld:pubmed |
pubmed-article:1785656 | pubmed:abstractText | A new screening method involving the multiplex polymerase chain reaction was developed to detect dystrophin gene deletions in Japanese patients with Duchenne and Becker muscular dystrophy (DMD/BMD). Eleven exonic regions including deletion "hot spots" were analyzed. Gene deletions were found in 33% of 92 unrelated Japanese patients, mainly in the central portion (exons 43-52) and at the 5' end (exons 1-17). This is a useful laboratory test for the rapid genetic diagnosis of DMD/BMD. | lld:pubmed |
pubmed-article:1785656 | pubmed:language | eng | lld:pubmed |
pubmed-article:1785656 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1785656 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:1785656 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1785656 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1785656 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:1785656 | pubmed:month | Sep | lld:pubmed |
pubmed-article:1785656 | pubmed:issn | 0387-7604 | lld:pubmed |
pubmed-article:1785656 | pubmed:author | pubmed-author:SuzukiYY | lld:pubmed |
pubmed-article:1785656 | pubmed:author | pubmed-author:YamadaHH | lld:pubmed |
pubmed-article:1785656 | pubmed:author | pubmed-author:IshiiKK | lld:pubmed |
pubmed-article:1785656 | pubmed:author | pubmed-author:SakurabaHH | lld:pubmed |
pubmed-article:1785656 | pubmed:author | pubmed-author:ShimmotoMM | lld:pubmed |
pubmed-article:1785656 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:1785656 | pubmed:volume | 13 | lld:pubmed |
pubmed-article:1785656 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:1785656 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:1785656 | pubmed:pagination | 339-42 | lld:pubmed |
pubmed-article:1785656 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:1785656 | pubmed:meshHeading | pubmed-meshheading:1785656-... | lld:pubmed |
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pubmed-article:1785656 | pubmed:meshHeading | pubmed-meshheading:1785656-... | lld:pubmed |
pubmed-article:1785656 | pubmed:meshHeading | pubmed-meshheading:1785656-... | lld:pubmed |
pubmed-article:1785656 | pubmed:meshHeading | pubmed-meshheading:1785656-... | lld:pubmed |
pubmed-article:1785656 | pubmed:year | 1991 | lld:pubmed |
pubmed-article:1785656 | pubmed:articleTitle | A screening for dystrophin gene deletions in Japanese patients with Duchenne/Becker muscular dystrophy by the multiplex polymerase chain reaction. | lld:pubmed |
pubmed-article:1785656 | pubmed:affiliation | Department of Clinical Genetics, Tokyo Metropolitan Institute of Medical Science, Japan. | lld:pubmed |
pubmed-article:1785656 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:1785656 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:1785656 | lld:pubmed |