Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2010-9-8
pubmed:abstractText
The risk of developing Wilms tumor (WT) can be present or absent in patients with nephrotic syndrome (NS) caused by WT1 mutations. Here, the genotype/phenotype correlation regarding the outcome and risk for WT in 52 patients from 51 families with NS due to WT1 mutations is described.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-10094551, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-10505700, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-10571943, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-11065340, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-11933209, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-12050205, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-12692171, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-1338906, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-14646409, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-14671061, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-14978175, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-15150775, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-15253707, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-16439601, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-1655284, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-16825260, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-16927106, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-17101338, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-17371932, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-18065803, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-18197032, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-19205749, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-19271246, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-20724521, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-2893190, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-2984395, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-3000666, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-4316066, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-7334749, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-9090524, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-9108089, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-9398852, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-9499425, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-9529364, http://linkedlifedata.com/resource/pubmed/commentcorrection/20595692-9607189
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1555-905X
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
5
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1655-62
pubmed:dateRevised
2011-9-13
pubmed:meshHeading
pubmed-meshheading:20595692-Humans, pubmed-meshheading:20595692-United States, pubmed-meshheading:20595692-Infant, pubmed-meshheading:20595692-Child, pubmed-meshheading:20595692-Kidney Neoplasms, pubmed-meshheading:20595692-Mutation, pubmed-meshheading:20595692-Child, Preschool, pubmed-meshheading:20595692-Female, pubmed-meshheading:20595692-Male, pubmed-meshheading:20595692-Wilms Tumor, pubmed-meshheading:20595692-Nephrotic Syndrome, pubmed-meshheading:20595692-Time Factors, pubmed-meshheading:20595692-Pedigree, pubmed-meshheading:20595692-Kidney Failure, Chronic, pubmed-meshheading:20595692-Phenotype, pubmed-meshheading:20595692-Karyotyping, pubmed-meshheading:20595692-Israel, pubmed-meshheading:20595692-Age of Onset, pubmed-meshheading:20595692-Turkey, pubmed-meshheading:20595692-Disease Progression, pubmed-meshheading:20595692-Risk Factors, pubmed-meshheading:20595692-Risk Assessment, pubmed-meshheading:20595692-Genetic Predisposition to Disease, pubmed-meshheading:20595692-Codon, Nonsense, pubmed-meshheading:20595692-Mutation, Missense, pubmed-meshheading:20595692-Sequence Deletion, pubmed-meshheading:20595692-Introns
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