| pubmed-article:2846283 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2846283 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:2846283 | lifeskim:mentions | umls-concept:C0029016 | lld:lifeskim |
| pubmed-article:2846283 | lifeskim:mentions | umls-concept:C0008533 | lld:lifeskim |
| pubmed-article:2846283 | lifeskim:mentions | umls-concept:C1442161 | lld:lifeskim |
| pubmed-article:2846283 | pubmed:issue | 9 | lld:pubmed |
| pubmed-article:2846283 | pubmed:dateCreated | 1988-12-21 | lld:pubmed |
| pubmed-article:2846283 | pubmed:abstractText | The mcf.2 transforming gene sequence has been located to the region between 29 and 61 kb 3' of the factor IX gene. Two unrelated haemophilia B patients who raise antibodies to infused factor IX ('inhibitors') have deletions in excess of 273 kb encompassing the factor IX and mcf.2 genes and a CG-rich island. We believe these patients show the first nullisomic deletion of a transforming gene to be reported. No clinical condition can be attributed to the loss of the mcf.2 gene. | lld:pubmed |
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| pubmed-article:2846283 | pubmed:language | eng | lld:pubmed |
| pubmed-article:2846283 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2846283 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:2846283 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2846283 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:2846283 | pubmed:issn | 0261-4189 | lld:pubmed |
| pubmed-article:2846283 | pubmed:author | pubmed-author:BirnbaumDD | lld:pubmed |
| pubmed-article:2846283 | pubmed:author | pubmed-author:BrownleeG GGG | lld:pubmed |
| pubmed-article:2846283 | pubmed:author | pubmed-author:BlakeD JDJ | lld:pubmed |
| pubmed-article:2846283 | pubmed:author | pubmed-author:AnikaM SMS | lld:pubmed |
| pubmed-article:2846283 | pubmed:author | pubmed-author:WinshipP RPR | lld:pubmed |
| pubmed-article:2846283 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2846283 | pubmed:volume | 7 | lld:pubmed |
| pubmed-article:2846283 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2846283 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2846283 | pubmed:pagination | 2795-9 | lld:pubmed |
| pubmed-article:2846283 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:2846283 | pubmed:year | 1988 | lld:pubmed |
| pubmed-article:2846283 | pubmed:articleTitle | Nullisomic deletion of the mcf.2 transforming gene in two haemophilia B patients. | lld:pubmed |
| pubmed-article:2846283 | pubmed:affiliation | Sir William Dunn School of Pathology, University of Oxford, UK. | lld:pubmed |
| pubmed-article:2846283 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:2846283 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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