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Titlebook: Hematologic Malignancies; Case Studies in Cyto Manorama Bhargava Book 2021 Springer Nature Singapore Pte Ltd. 2021 Case studies in Hematolo

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41#
發(fā)表于 2025-3-28 17:07:40 | 只看該作者
rceived by the citing author. The collective view of a large number of citing authors regarding the relationships between documents represented by citations, that is the ., can therefore be analyzed to study the intellectual structures of research fields, and to inform knowledge organization and inf
42#
發(fā)表于 2025-3-28 20:23:33 | 只看該作者
Manorama Bhargava or research field during a certain time period. The first step in a citation network analysis study is therefore to collect a set of citing papers (along with their reference lists) to represent a defined scholarly community or research field within a specified time period (which is called a .). Th
43#
發(fā)表于 2025-3-29 01:54:58 | 只看該作者
44#
發(fā)表于 2025-3-29 04:54:26 | 只看該作者
45#
發(fā)表于 2025-3-29 08:45:51 | 只看該作者
Manorama Bhargavaale citation analysis, even without special access to special data collections. Exciting new developments are emerging this way in many aspects of citation analysis. This book critically examines both theory and practical techniques of citation network analysis and visualization, one of the two main
46#
發(fā)表于 2025-3-29 12:51:01 | 只看該作者
Manorama Bhargavaation that arises in any network utility maximization. .In the high power regime, a simple characterization of the obtained performance becomes possible due to the fact that the weighted sum rate utility conver978-3-642-43634-5978-3-642-31692-0Series ISSN 1863-8538 Series E-ISSN 1863-8546
47#
發(fā)表于 2025-3-29 16:24:10 | 只看該作者
48#
發(fā)表于 2025-3-29 23:05:46 | 只看該作者
Acute Myeloid Leukemiaive AML: AML with mutated NPM1 and AML with biallelic CEBPA mutations. AML with RUNX1 mutation and AML with BCR-ABL1 fusion have been added as provisional entities in the WHO classification (2016)..The following 33 case studies include all categories seen in AML: Recurrent cytogenetic abnormalities,
49#
發(fā)表于 2025-3-30 00:49:47 | 只看該作者
Myelodysplastic Syndromeence of diagnostic morphologic features of MDS. del(5q) remains as the only cytogenetic abnormality that defines a specific MDS subtype..The following case studies on MDS describe the various permutations and combinations of genetic abnormalities conforming to the WHO classification for MDS (2016) (
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