pubmed-article:2213160 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:2213160 | lifeskim:mentions | umls-concept:C0006118 | lld:lifeskim |
pubmed-article:2213160 | lifeskim:mentions | umls-concept:C0795878 | lld:lifeskim |
pubmed-article:2213160 | lifeskim:mentions | umls-concept:C0205182 | lld:lifeskim |
pubmed-article:2213160 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:2213160 | pubmed:dateCreated | 1990-11-21 | lld:pubmed |
pubmed-article:2213160 | pubmed:abstractText | Cytogenetic studies of three rare childhood brain tumors were performed. Two children presented with pure rhabdoid tumors. The third child had a tumor composed of a mixture of rhabdoid elements with neuroepithelial, epithelial, and mesenchymal tissue - an atypical teratoid tumor. All three tumors demonstrated monosomy 22 as the only cytogenetic abnormality. The cytogenetic findings suggest that loss of a gene or genes on chromosome 22 may be involved in the initiation or progression of these malignant tumors. Further studies on additional fresh tumor specimens are warranted; however, it is possible that cytogenetic studies may be used as an additional means of diagnosing rhabdoid or atypical teratoid tumors of the brain. | lld:pubmed |
pubmed-article:2213160 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2213160 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2213160 | pubmed:language | eng | lld:pubmed |
pubmed-article:2213160 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2213160 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:2213160 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:2213160 | pubmed:month | Nov | lld:pubmed |
pubmed-article:2213160 | pubmed:issn | 0022-3085 | lld:pubmed |
pubmed-article:2213160 | pubmed:author | pubmed-author:EmanuelB SBS | lld:pubmed |
pubmed-article:2213160 | pubmed:author | pubmed-author:RorkeL BLB | lld:pubmed |
pubmed-article:2213160 | pubmed:author | pubmed-author:PackerR JRJ | lld:pubmed |
pubmed-article:2213160 | pubmed:author | pubmed-author:BiegelJ AJA | lld:pubmed |
pubmed-article:2213160 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:2213160 | pubmed:volume | 73 | lld:pubmed |
pubmed-article:2213160 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:2213160 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:2213160 | pubmed:pagination | 710-4 | lld:pubmed |
pubmed-article:2213160 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
pubmed-article:2213160 | pubmed:meshHeading | pubmed-meshheading:2213160-... | lld:pubmed |
pubmed-article:2213160 | pubmed:meshHeading | pubmed-meshheading:2213160-... | lld:pubmed |
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pubmed-article:2213160 | pubmed:meshHeading | pubmed-meshheading:2213160-... | lld:pubmed |
pubmed-article:2213160 | pubmed:meshHeading | pubmed-meshheading:2213160-... | lld:pubmed |
pubmed-article:2213160 | pubmed:meshHeading | pubmed-meshheading:2213160-... | lld:pubmed |
pubmed-article:2213160 | pubmed:meshHeading | pubmed-meshheading:2213160-... | lld:pubmed |
pubmed-article:2213160 | pubmed:meshHeading | pubmed-meshheading:2213160-... | lld:pubmed |
pubmed-article:2213160 | pubmed:meshHeading | pubmed-meshheading:2213160-... | lld:pubmed |
pubmed-article:2213160 | pubmed:meshHeading | pubmed-meshheading:2213160-... | lld:pubmed |
pubmed-article:2213160 | pubmed:meshHeading | pubmed-meshheading:2213160-... | lld:pubmed |
pubmed-article:2213160 | pubmed:year | 1990 | lld:pubmed |
pubmed-article:2213160 | pubmed:articleTitle | Monosomy 22 in rhabdoid or atypical tumors of the brain. | lld:pubmed |
pubmed-article:2213160 | pubmed:affiliation | Division of Human Genetics and Molecular Biology, Children's Hospital of Philadelphia, Pennsylvania. | lld:pubmed |
pubmed-article:2213160 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:2213160 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:2213160 | pubmed:publicationType | Case Reports | lld:pubmed |
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