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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1992-2-4
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pubmed:abstractText |
Chromosome analysis of bone marrow aspirate from a 46-year-old man with acute promyelocytic leukemia (APL) revealed a variant translocation, 46,XY,t(1:15;17)(p36;q22;q21.1). The breakpoints in chromosomes 15 and 17 appear to be the same as those in the more common translocation, t(15;17), associated with APL. The common translocation has been reported in up to 80% of cases of APL. Seventeen cases with variant translocations have been reported involving 15 alone, 17 alone, or 15, 17, and some other chromosome.
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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 |
Dec
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pubmed:issn |
0165-4608
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
57
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
201-7
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pubmed:dateRevised |
2005-11-16
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pubmed:meshHeading |
pubmed-meshheading:1756499-Chromosome Aberrations,
pubmed-meshheading:1756499-Chromosome Disorders,
pubmed-meshheading:1756499-Chromosomes, Human, Pair 1,
pubmed-meshheading:1756499-Chromosomes, Human, Pair 15,
pubmed-meshheading:1756499-Chromosomes, Human, Pair 17,
pubmed-meshheading:1756499-Humans,
pubmed-meshheading:1756499-Karyotyping,
pubmed-meshheading:1756499-Leukemia, Promyelocytic, Acute,
pubmed-meshheading:1756499-Male,
pubmed-meshheading:1756499-Middle Aged,
pubmed-meshheading:1756499-Translocation, Genetic
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pubmed:year |
1991
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pubmed:articleTitle |
Report of a variant t(1;15;17)(p36;q22;q21.1) in a patient with acute promyelocytic leukemia.
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pubmed:affiliation |
Center for Human Genetics, Boston University, Massachusetts.
|
pubmed:publicationType |
Journal Article,
Review,
Case Reports
|