Statements in which the resource exists.
SubjectPredicateObjectContext
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pubmed-article:10073911pubmed:abstractTextPrenatal diagnosis of Duchenne and Becker muscular dystrophy (DMD) is performed as a routine procedure in many laboratories. The major potential problem is an incorrect diagnosis that could be obtained due to contamination with maternal tissue. We report a case of mosaicism of the X-chromosomes confined to the placenta as a possible source of confusing results in prenatal diagnosis of DMD. To the best of our knowledge, this is the first reported case of this problem in a prenatal DMD diagnosis.lld:pubmed
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pubmed-article:10073911pubmed:authorpubmed-author:WolfCClld:pubmed
pubmed-article:10073911pubmed:authorpubmed-author:ThieleHHlld:pubmed
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pubmed-article:10073911pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:10073911pubmed:year1999lld:pubmed
pubmed-article:10073911pubmed:articleTitlePitfalls in prenatal diagnosis of DMD due to placental mosaicism of the X-chromosomes: prenatal and postnatal findings in a fetus with a deletion of exons 67-71 of the dystrophin gene.lld:pubmed
pubmed-article:10073911pubmed:affiliationInstitut für Humangenetik, Universität Leipzig, Germany.lld:pubmed
pubmed-article:10073911pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10073911pubmed:publicationTypeCase Reportslld:pubmed