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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
1983-7-29
|
| pubmed:abstractText |
Cytogenetic examination of multiple peripheral blood cultures of a patient with myelofibrosis with myeloid metaplasia revealed the presence of an interstitial deletion of the long arm of chromosome 11, del(11)(q13q21). A folic acid dependent fragile site fra(11)(q13) was found in about 12% of the cells. The possible correlation between constitutional fragile site and acquired chromosomal alteration is discussed briefly.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0340-6717
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
63
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
299-301
|
| pubmed:dateRevised |
2008-11-21
|
| pubmed:meshHeading |
pubmed-meshheading:6852829-Chromosome Deletion,
pubmed-meshheading:6852829-Chromosome Fragile Sites,
pubmed-meshheading:6852829-Chromosome Fragility,
pubmed-meshheading:6852829-Chromosomes, Human, 6-12 and X,
pubmed-meshheading:6852829-Female,
pubmed-meshheading:6852829-Humans,
pubmed-meshheading:6852829-Middle Aged,
pubmed-meshheading:6852829-Primary Myelofibrosis
|
| pubmed:year |
1983
|
| pubmed:articleTitle |
Coincidence between fragile site expression and interstitial deletion of chromosome 11 in a case of myelofibrosis.
|
| pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|