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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
5 Pt 1
|
| pubmed:dateCreated |
1993-6-23
|
| pubmed:abstractText |
The development of Wilms tumor in a patient with Prader-Willi syndrome prompted us to determine the parental origin of the genes implicated in both disorders because of the sex-specific parent-of-origin effects previously demonstrated for both conditions. A paternal chromosome 15q11-q13 deletion was demonstrated, but no changes were demonstrated in a limited analysis of chromosome 11p, which harbors two Wilms tumor suppressor genes, WT1 and WT2.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
AIM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
May
|
| pubmed:issn |
0022-3476
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
122
|
| pubmed:geneSymbol |
WT1,
WT2
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
730-3
|
| pubmed:dateRevised |
2005-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:8388447-Chromosome Deletion,
pubmed-meshheading:8388447-Chromosomes, Human, Pair 11,
pubmed-meshheading:8388447-Humans,
pubmed-meshheading:8388447-Infant,
pubmed-meshheading:8388447-Kidney Neoplasms,
pubmed-meshheading:8388447-Male,
pubmed-meshheading:8388447-Prader-Willi Syndrome,
pubmed-meshheading:8388447-Wilms Tumor
|
| pubmed:year |
1993
|
| pubmed:articleTitle |
Wilms tumor in a patient with Prader-Willi syndrome.
|
| pubmed:affiliation |
Department of Cancer Biology, Cleveland Clinic Foundation, Ohio.
|
| pubmed:publicationType |
Journal Article,
Review,
Case Reports
|