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rdf:type |
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|
lifeskim:mentions |
|
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pubmed:issue |
1
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pubmed:dateCreated |
1998-6-2
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pubmed:abstractText |
A case of Waldenstrom macroglobulinemia with Burkitt-type t(8;14)(q24.1;q32) and total and partial trisomy 3 is reported. This is an unusual combination of chromosomal abnormalities in Waldenstrom macroglobulinemia.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0165-4608
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
103
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
65-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9595048-Aged,
pubmed-meshheading:9595048-Chromosomes, Human, Pair 14,
pubmed-meshheading:9595048-Chromosomes, Human, Pair 3,
pubmed-meshheading:9595048-Chromosomes, Human, Pair 8,
pubmed-meshheading:9595048-Humans,
pubmed-meshheading:9595048-Karyotyping,
pubmed-meshheading:9595048-Male,
pubmed-meshheading:9595048-Pleural Effusion,
pubmed-meshheading:9595048-Translocation, Genetic,
pubmed-meshheading:9595048-Trisomy,
pubmed-meshheading:9595048-Waldenstrom Macroglobulinemia
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pubmed:year |
1998
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|
pubmed:articleTitle |
A case of t(8;14) with total and partial trisomy 3 in Waldenstrom macroglobulinemia.
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pubmed:affiliation |
Department of Pathology, Singapore General Hospital, Republic of Singapore.
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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