|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
7
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|
pubmed:dateCreated |
1999-8-24
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|
pubmed:abstractText |
Mantle cell lymphomas (MCLs) comprise a rare but distinct clinicopathological entity usually associated with t(11;14). This translocation is regarded as a primary event, but it has been suggested that other as yet unidentified genetic alterations are required for development and progression of MCL.
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pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Jul
|
|
pubmed:issn |
0390-6078
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
84
|
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
594-9
|
|
pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:10406899-Chromosome Aberrations,
pubmed-meshheading:10406899-Chromosome Disorders,
pubmed-meshheading:10406899-Chromosomes, Human, Pair 11,
pubmed-meshheading:10406899-Chromosomes, Human, Pair 14,
pubmed-meshheading:10406899-Humans,
pubmed-meshheading:10406899-Karyotyping,
pubmed-meshheading:10406899-Lymphoma, Non-Hodgkin,
pubmed-meshheading:10406899-Translocation, Genetic
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|
pubmed:year |
1999
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|
pubmed:articleTitle |
Secondary chromosome changes in mantle cell lymphoma.
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|
pubmed:affiliation |
Centre for Human Genetics, Herestraat 49, B-3000 Leuven, Belgium.
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|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
