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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1983-8-26
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pubmed:abstractText |
A balanced paternal chromosome insertion, ins(11) p14q14q21, resulted in a female with an unbalanced karyotype, del(11)(q14q21). This imbalance presumably arose from a meiotic crossover between the breakpoint of the insertion and the breakpoints of the deletion. This child developed a malignant lymphoma of the thymus in the first year of life. The association of a lymphoma with an 11q deletion may not be a coincidence in view of the frequent involvement of 11q in cytogenetic alterations of lymphomas.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
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pubmed:issn |
0340-6717
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
63
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
323-6
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:6688062-Chromosome Deletion,
pubmed-meshheading:6688062-Chromosomes, Human, 6-12 and X,
pubmed-meshheading:6688062-Female,
pubmed-meshheading:6688062-Humans,
pubmed-meshheading:6688062-Infant,
pubmed-meshheading:6688062-Karyotyping,
pubmed-meshheading:6688062-Lymphoma, Non-Hodgkin,
pubmed-meshheading:6688062-Mediastinal Neoplasms
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pubmed:year |
1983
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pubmed:articleTitle |
The association of a lymphoreticular malignancy with an 11q deletion: a coincidence or a cancer susceptibility?
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pubmed:publicationType |
Journal Article,
Case Reports
|