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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1997-12-10
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pubmed:abstractText |
Renal oncocytomas reveal a considerable (cyto)genetic heterogeneity. At least 2 genetic subsets are currently recognized, characterized by (1) translocations involving breakpoint 11q13 and (2) the combined loss of chromosomes 1 and X/Y. We present a case of oncocytoma revealing a 3-way translocation involving breakpoint 11q13, a der(1)t(1;8) and an add(19). The der(1) resulted in loss of chromosome 1 sequences. Using fluorescence in situ hybridization, the 11q13 breakpoint of the present case proved to be slightly different from the one observed previously in 3 cases of renal oncocytoma. Whether the 11q13 breakpoint observed in our case resides in or near another gene remains to be elucidated.
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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 |
Nov
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pubmed:issn |
0020-7136
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
14
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pubmed:volume |
73
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
521-4
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pubmed:dateRevised |
2007-7-24
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pubmed:meshHeading |
pubmed-meshheading:9389566-Adenoma, Oxyphilic,
pubmed-meshheading:9389566-Chromosome Deletion,
pubmed-meshheading:9389566-Chromosomes, Human, Pair 1,
pubmed-meshheading:9389566-Chromosomes, Human, Pair 11,
pubmed-meshheading:9389566-Chromosomes, Human, Pair 12,
pubmed-meshheading:9389566-Chromosomes, Human, Pair 19,
pubmed-meshheading:9389566-Chromosomes, Human, Pair 5,
pubmed-meshheading:9389566-Chromosomes, Human, Pair 8,
pubmed-meshheading:9389566-Humans,
pubmed-meshheading:9389566-Kidney Neoplasms,
pubmed-meshheading:9389566-Male,
pubmed-meshheading:9389566-Middle Aged,
pubmed-meshheading:9389566-Translocation, Genetic
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pubmed:year |
1997
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pubmed:articleTitle |
Renal oncocytoma with t(5;12;11), der(1)1;8) and add(19): "true" oncocytoma or chromophobe adenoma?
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pubmed:affiliation |
Department of Medical Genetics, University of Groningen, The Netherlands. T.Dijkhuizen@med.rug.nl
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pubmed:publicationType |
Journal Article,
Case Reports
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