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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2011-3-24
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pubmed:abstractText |
JAK2 V617F mutation is gaining more acceptance in laboratory testing as part of the differential diagnosis work-up of myeloproliferative disorders (MPD). This report is the first of its kind from Lebanon that analyzes the distribution of this mutation among a series of referred cases to a major tertiary referral center.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1945-0257
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
263-5
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pubmed:meshHeading |
pubmed-meshheading:21198321-Adult,
pubmed-meshheading:21198321-Humans,
pubmed-meshheading:21198321-Janus Kinase 2,
pubmed-meshheading:21198321-Lebanon,
pubmed-meshheading:21198321-Mutation,
pubmed-meshheading:21198321-Myeloproliferative Disorders,
pubmed-meshheading:21198321-Polycythemia Vera,
pubmed-meshheading:21198321-Polymerase Chain Reaction,
pubmed-meshheading:21198321-Referral and Consultation,
pubmed-meshheading:21198321-Thrombocythemia, Essential
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pubmed:year |
2011
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pubmed:articleTitle |
JAK2 V617F gene mutation in the laboratory work-up of myeloproliferative disorders: experience of a major referral center in Lebanon.
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pubmed:affiliation |
Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Beirut, Lebanon. rm11@aub.edu.lb
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pubmed:publicationType |
Journal Article
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