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pubmed-article:9527951pubmed:abstractTextChromosomal analysis of fetal cells is a commonly used, safe, and highly accurate procedure. The rate of false-negative results is unknown. Recent experience at four centers suggests that there may be a particular likelihood for mosaic trisomy 8 to be missed with routine antenatal diagnostic procedures. This report reviews these cases, the characteristic findings of mosaic trisomy 8, and the tissue-specific differential yield of chromosomal analysis that may contribute to the increased risk of missed antenatal diagnosis in patients with this disorder.lld:pubmed
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pubmed-article:9527951pubmed:authorpubmed-author:PaiG SGSlld:pubmed
pubmed-article:9527951pubmed:authorpubmed-author:WagnerC LCLlld:pubmed
pubmed-article:9527951pubmed:authorpubmed-author:CantúE SESlld:pubmed
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pubmed-article:9527951pubmed:authorpubmed-author:ShieldsS MSMlld:pubmed
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pubmed-article:9527951pubmed:pagination78-80lld:pubmed
pubmed-article:9527951pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:9527951pubmed:articleTitleMosaic trisomy 8: a cautionary note regarding missed antenatal diagnosis.lld:pubmed
pubmed-article:9527951pubmed:affiliationDepartment of Pediatrics, Medical University of South Carolina, Charleston 29425, USA.lld:pubmed
pubmed-article:9527951pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9527951pubmed:publicationTypeCase Reportslld:pubmed