Source:http://linkedlifedata.com/resource/pubmed/id/10214502
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1999-5-18
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pubmed:abstractText |
The 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.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0003-3995
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
11-5
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10214502-Adolescent,
pubmed-meshheading:10214502-Adult,
pubmed-meshheading:10214502-Child,
pubmed-meshheading:10214502-Child, Preschool,
pubmed-meshheading:10214502-Chromosomes, Human, Pair 21,
pubmed-meshheading:10214502-Down Syndrome,
pubmed-meshheading:10214502-Female,
pubmed-meshheading:10214502-Genomic Imprinting,
pubmed-meshheading:10214502-Humans,
pubmed-meshheading:10214502-Infant,
pubmed-meshheading:10214502-Infant, Newborn,
pubmed-meshheading:10214502-Male,
pubmed-meshheading:10214502-Meiosis,
pubmed-meshheading:10214502-Nondisjunction, Genetic,
pubmed-meshheading:10214502-Parents,
pubmed-meshheading:10214502-Polymorphism, Genetic,
pubmed-meshheading:10214502-Sex Ratio,
pubmed-meshheading:10214502-Trisomy
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pubmed:year |
1999
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pubmed:articleTitle |
Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21.
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pubmed:affiliation |
Genetics Service, Hospital Clínic, Barcelona, Spain.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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