Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1985-8-21
|
| pubmed:abstractText |
A 2-year-old girl with sporadic unilateral Wilms' tumor (WT) not associated with aniridia was found to have, besides other chromosome abnormalities, a t(2;7)(q33;p22) in 6% of her lymphocytes. A comparison with 7 previous WT cases without aniridia in whom diverse chromosomal aberrations were present, reveals a wide heterogeneity and lead us to tentatively classify such changes as causal, secondary, and casual.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0003-3995
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
28
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
52-4
|
| pubmed:dateRevised |
2005-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:2990318-Child, Preschool,
pubmed-meshheading:2990318-Chromosomes, Human, 1-3,
pubmed-meshheading:2990318-Chromosomes, Human, 6-12 and X,
pubmed-meshheading:2990318-Female,
pubmed-meshheading:2990318-Humans,
pubmed-meshheading:2990318-Karyotyping,
pubmed-meshheading:2990318-Mosaicism,
pubmed-meshheading:2990318-Wilms Tumor
|
| pubmed:year |
1985
|
| pubmed:articleTitle |
Constitutional mosaic t(2;7)(q33;p22) and other rearrangements in a girl with Wilms' tumor.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|