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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1996-5-15
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pubmed:abstractText |
Trisomy 12 and deletions or translocations of 13q14 are the commonest cytogenetic abnormalities in chronic lymphocytic leukaemia but rarely co-exist in the same patient. We describe eight patients from a series of > 400 patients with CLL in whom trisomy 12 and t or del 13 occur in the same clone. Using FISH we have identified clones with trisomy 12 alone, t or del 13q14 alone and both abnormalities, in each of the patients studied. This implies that neither trisomy 12 nor t or del 13q14 is the initiating event in leukaemogenesis, but does not exclude the possibility of a submicroscopic abnormality of 13q14 occurring as an early event.
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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:month |
Feb
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pubmed:issn |
0007-1048
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
92
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
389-92
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:8603005-Aged,
pubmed-meshheading:8603005-Aged, 80 and over,
pubmed-meshheading:8603005-Chromosomes, Human, Pair 12,
pubmed-meshheading:8603005-Chromosomes, Human, Pair 13,
pubmed-meshheading:8603005-Female,
pubmed-meshheading:8603005-Gene Deletion,
pubmed-meshheading:8603005-Humans,
pubmed-meshheading:8603005-In Situ Hybridization, Fluorescence,
pubmed-meshheading:8603005-Karyotyping,
pubmed-meshheading:8603005-Leukemia, Lymphocytic, Chronic, B-Cell,
pubmed-meshheading:8603005-Male,
pubmed-meshheading:8603005-Middle Aged,
pubmed-meshheading:8603005-Translocation, Genetic,
pubmed-meshheading:8603005-Trisomy
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pubmed:year |
1996
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pubmed:articleTitle |
Trisomy 12 and structural abnormalities of 13q14 occurring in the same clone in chronic lymphocytic leukaemia.
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pubmed:affiliation |
Department of Haematology, Royal Bournemouth Hospital.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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