Acute myeloid leukemia (AML-M2) with translocation (8;21) (q22;q22) and abnormal eosinophilic precursors in the bone marrow-A case report
Indian Journal of Pediatrics, ISSN: 0973-7693, Vol: 79, Issue: 2, Page: 256-259
2012
- 2Citations
- 3Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations2
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- CrossRef1
- Captures3
- Readers3
Article Description
The translocation (8;21)(q22;q22) is frequently associated with M2 subtype of AML. The authors herein present a case of AML-M2 in a nine-year-old boy without hepatosplenomegaly, lymphadenopathy or any bleeding diathesis. Bone marrow examination revealed high number of eosinophilic precursors (60%) among the total nucleated bone marrow cells. Cytogenetic study with G- banding method showed 46, XY, t (8;21)(q22;q22). The morphological abnormalities in eosinophils observed in AML suggested that eosinophils may be a part of leukemic process. © Dr. K C Chaudhuri Foundation 2011.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84861519939&origin=inward; http://dx.doi.org/10.1007/s12098-011-0481-2; http://www.ncbi.nlm.nih.gov/pubmed/21630067; http://link.springer.com/10.1007/s12098-011-0481-2; https://dx.doi.org/10.1007/s12098-011-0481-2; https://link.springer.com/article/10.1007/s12098-011-0481-2; http://www.springerlink.com/index/10.1007/s12098-011-0481-2; http://www.springerlink.com/index/pdf/10.1007/s12098-011-0481-2
Springer Science and Business Media LLC
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