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pubmed-article:14743650pubmed:dateCreated2004-1-27lld:pubmed
pubmed-article:14743650pubmed:abstractTextA specific genetic diagnosis can be reached for most children with muscular dystrophy. Advanced diagnostics, including genetic testing and analysis of nonmuscle tissues, such as skin and blood, often allow the diagnosis to be reached using minimally invasive procedures. These diagnostic advances accompany improved understanding of pathophysiology and pave the way for specific and curative treatments.lld:pubmed
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pubmed-article:14743650pubmed:issn0733-8619lld:pubmed
pubmed-article:14743650pubmed:authorpubmed-author:MathewsKather...lld:pubmed
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pubmed-article:14743650pubmed:volume21lld:pubmed
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pubmed-article:14743650pubmed:pagination795-816lld:pubmed
pubmed-article:14743650pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:14743650pubmed:year2003lld:pubmed
pubmed-article:14743650pubmed:articleTitleMuscular dystrophy overview: genetics and diagnosis.lld:pubmed
pubmed-article:14743650pubmed:affiliationDepartment of Pediatrics, University of Iowa, 200 Hawkins Drive, Iowa City, IA 52240, USA. katherine-mathews@uiowa.edulld:pubmed
pubmed-article:14743650pubmed:publicationTypeJournal Articlelld:pubmed
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