17943164

Source:http://linkedlifedata.com/resource/pubmed/id/17943164

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008625, umls-concept:C0023487, umls-concept:C0034897, umls-concept:C0314603, umls-concept:C0332257, umls-concept:C1414333, umls-concept:C1524062, umls-concept:C1880022, umls-concept:C2827473
pubmed:issue	4
pubmed:dateCreated	2008-4-16
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8704895
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1476-5551
pubmed:author	pubmed-author:AxH AHA, pubmed-author:ChoBB, pubmed-author:ChungN GNG, pubmed-author:FoxJ HJH, pubmed-author:FoyS PSP, pubmed-author:KimH KHK, pubmed-author:KimMM, pubmed-author:KimYY, pubmed-author:LeeD HDH, pubmed-author:LinKK, pubmed-author:MinW-SWS
pubmed:issnType	Electronic
pubmed:volume	22
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	881-3
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:17943164-Chromosome Aberrations, pubmed-meshheading:17943164-Chromosome Inversion, pubmed-meshheading:17943164-Chromosomes, Human, Pair 15, pubmed-meshheading:17943164-Chromosomes, Human, Pair 17, pubmed-meshheading:17943164-Humans, pubmed-meshheading:17943164-Leukemia, Promyelocytic, Acute, pubmed-meshheading:17943164-Translocation, Genetic
pubmed:year	2008
pubmed:articleTitle	The genetic characterization of acute promyelocytic leukemia with cryptic t(15;17) including a new recurrent additional cytogenetic abnormality i(17)(q10).
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't