| pubmed-article:15641267 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15641267 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:15641267 | lifeskim:mentions | umls-concept:C0026850 | lld:lifeskim |
| pubmed-article:15641267 | lifeskim:mentions | umls-concept:C1442161 | lld:lifeskim |
| pubmed-article:15641267 | lifeskim:mentions | umls-concept:C1707520 | lld:lifeskim |
| pubmed-article:15641267 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:15641267 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
| pubmed-article:15641267 | lifeskim:mentions | umls-concept:C1704666 | lld:lifeskim |
| pubmed-article:15641267 | lifeskim:mentions | umls-concept:C1517892 | lld:lifeskim |
| pubmed-article:15641267 | lifeskim:mentions | umls-concept:C0208973 | lld:lifeskim |
| pubmed-article:15641267 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:15641267 | pubmed:dateCreated | 2005-1-11 | lld:pubmed |
| pubmed-article:15641267 | pubmed:abstractText | We carried out molecular deletion analysis on 142 patients with Duchenne/Becker muscular dystrophy which covered 25 exons of the dystrophin gene. We also evaluated the results by comparing with the clinical findings and examples in the literature. A deletion ratio of 63.7% was achieved. Exon 46 was the most frequently affected region. Interestingly we also observed four cases with muscle promoter (Mp) region deletions which have been rarely reported in the literature. | lld:pubmed |
| pubmed-article:15641267 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15641267 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15641267 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15641267 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15641267 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15641267 | pubmed:issn | 0041-4301 | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:OzkinayFerdaF | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:KurulSemraS | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:UlgenalpAyfer... | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:DirikErayE | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:UranNedretN | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:BoraElçinE | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:ErçalDeryaD | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:Tütüncüo?luSa... | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:KarasoyHatice... | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:GirayOzlemO | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:HizliTülinT | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:Sa?in-SaylamG... | lld:pubmed |
| pubmed-article:15641267 | pubmed:author | pubmed-author:DizdarerGül?e... | lld:pubmed |
| pubmed-article:15641267 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15641267 | pubmed:volume | 46 | lld:pubmed |
| pubmed-article:15641267 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15641267 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15641267 | pubmed:pagination | 333-8 | lld:pubmed |
| pubmed-article:15641267 | pubmed:meshHeading | pubmed-meshheading:15641267... | lld:pubmed |
| pubmed-article:15641267 | pubmed:meshHeading | pubmed-meshheading:15641267... | lld:pubmed |
| pubmed-article:15641267 | pubmed:meshHeading | pubmed-meshheading:15641267... | lld:pubmed |
| pubmed-article:15641267 | pubmed:meshHeading | pubmed-meshheading:15641267... | lld:pubmed |
| pubmed-article:15641267 | pubmed:meshHeading | pubmed-meshheading:15641267... | lld:pubmed |
| pubmed-article:15641267 | pubmed:meshHeading | pubmed-meshheading:15641267... | lld:pubmed |
| pubmed-article:15641267 | pubmed:meshHeading | pubmed-meshheading:15641267... | lld:pubmed |
| pubmed-article:15641267 | pubmed:meshHeading | pubmed-meshheading:15641267... | lld:pubmed |
| pubmed-article:15641267 | pubmed:meshHeading | pubmed-meshheading:15641267... | lld:pubmed |
| pubmed-article:15641267 | pubmed:meshHeading | pubmed-meshheading:15641267... | lld:pubmed |
| pubmed-article:15641267 | pubmed:meshHeading | pubmed-meshheading:15641267... | lld:pubmed |
| pubmed-article:15641267 | pubmed:meshHeading | pubmed-meshheading:15641267... | lld:pubmed |
| pubmed-article:15641267 | pubmed:articleTitle | Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy. | lld:pubmed |
| pubmed-article:15641267 | pubmed:affiliation | Department of Pediatrics, Dokuz Eylül University Faculty of Medicine, Izmir, Turkey. | lld:pubmed |
| pubmed-article:15641267 | pubmed:publicationType | Journal Article | lld:pubmed |
