Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:3195282rdf:typepubmed:Citationlld:pubmed
pubmed-article:3195282lifeskim:mentionsumls-concept:C0026850lld:lifeskim
pubmed-article:3195282lifeskim:mentionsumls-concept:C0085862lld:lifeskim
pubmed-article:3195282lifeskim:mentionsumls-concept:C1299583lld:lifeskim
pubmed-article:3195282lifeskim:mentionsumls-concept:C1744681lld:lifeskim
pubmed-article:3195282lifeskim:mentionsumls-concept:C0596611lld:lifeskim
pubmed-article:3195282lifeskim:mentionsumls-concept:C1442161lld:lifeskim
pubmed-article:3195282lifeskim:mentionsumls-concept:C0205195lld:lifeskim
pubmed-article:3195282lifeskim:mentionsumls-concept:C1608386lld:lifeskim
pubmed-article:3195282lifeskim:mentionsumls-concept:C1549571lld:lifeskim
pubmed-article:3195282pubmed:issue8lld:pubmed
pubmed-article:3195282pubmed:dateCreated1988-12-23lld:pubmed
pubmed-article:3195282pubmed:abstractTextThe authors describe a combination of Duchenne muscular dystrophy and congenital ichthyosis in a 6.5-year-old boy. This is the first ever description appearing in the world literature. The authors discuss possible variants of mutation (either chromosomal aberration or two independent gene mutations in chromosome 21).lld:pubmed
pubmed-article:3195282pubmed:languageruslld:pubmed
pubmed-article:3195282pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3195282pubmed:citationSubsetIMlld:pubmed
pubmed-article:3195282pubmed:statusMEDLINElld:pubmed
pubmed-article:3195282pubmed:issn0044-4588lld:pubmed
pubmed-article:3195282pubmed:authorpubmed-author:BadalianL OLOlld:pubmed
pubmed-article:3195282pubmed:authorpubmed-author:TeminP APAlld:pubmed
pubmed-article:3195282pubmed:authorpubmed-author:KamennykhL...lld:pubmed
pubmed-article:3195282pubmed:authorpubmed-author:ArkhipovB ABAlld:pubmed
pubmed-article:3195282pubmed:authorpubmed-author:ZavadenkoN...lld:pubmed
pubmed-article:3195282pubmed:issnTypePrintlld:pubmed
pubmed-article:3195282pubmed:volume88lld:pubmed
pubmed-article:3195282pubmed:ownerNLMlld:pubmed
pubmed-article:3195282pubmed:authorsCompleteYlld:pubmed
pubmed-article:3195282pubmed:pagination48-51lld:pubmed
pubmed-article:3195282pubmed:dateRevised2010-11-18lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:meshHeadingpubmed-meshheading:3195282-...lld:pubmed
pubmed-article:3195282pubmed:year1988lld:pubmed
pubmed-article:3195282pubmed:articleTitle[A combination of Duchenne's progressive muscular dystrophy with congenital ichthyosis--a deletion or 2 independent gene mutations at Xp21--Xp22?].lld:pubmed
pubmed-article:3195282pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3195282pubmed:publicationTypeEnglish Abstractlld:pubmed
pubmed-article:3195282pubmed:publicationTypeCase Reportslld:pubmed