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pubmed-article:10214502pubmed:abstractTextThe parental origin and the meiotic stage of non-disjunction have been determined in 139 Down syndrome patients with regular trisomy 21 and in their parents through the analysis of DNA polymorphism. The meiotic error is maternal in 91.60% cases and paternal in 8.39% of cases. Of the maternal cases, 72.41% were due to meiosis I errors (MMI) and 27.58% were due to meiosis II errors (MMII). Of the paternal cases, 45.45% were due to meiosis I (PMI) and 54.54% were due to meiosis II (PMII). The mean maternal ages were 31.6 +/- 5.3 (+/- SD) years in errors from MMI, 32.3 +/- 6.4 years in errors from MMII, 31.4 +/- 4.6 years in errors from PMI and 29.5 +/- 2.7 years in errors from PMII. No significant statistical differences were observed between maternal and paternal errors, further supporting the presence of a constant chromosome 21 non-disjunction error type.lld:pubmed
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pubmed-article:10214502pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:10214502pubmed:year1999lld:pubmed
pubmed-article:10214502pubmed:articleTitleParental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21.lld:pubmed
pubmed-article:10214502pubmed:affiliationGenetics Service, Hospital Clínic, Barcelona, Spain.lld:pubmed
pubmed-article:10214502pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10214502pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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