FLT3/D835 mutation and inversion of chromosome 16 in leukemic transformation of myelofibrosis
Author:
Publisher
Elsevier BV
Subject
Internal Medicine
Reference6 articles.
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2. Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies;Yamamoto;Blood,2001
3. A multiplex RT-PCR assay for detection of chimeric transcripts encoded risk-stratifying translocation of pediatric acute lymphoblastic leukemia;Scurto;Leukemia,1998
4. Incidence and prognosis of c-KIT and FLT3 mutations in core binding factor (CBF) acute myeloid leukemias;Care;Br J Haematol,2003
5. Circulation haematopoietic progenitor cells in primary and secondary myelofibrosis: relation to collagen and reticulin fibrosis;Colovic;Eur J Haematol,1999
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2. Analysis of Chromosomal Aberrations and FLT3 gene Mutations in Childhood Acute Myelogenous Leukemia Patients;Turkish Journal of Hematology;2012
3. Acute Myeloid Leukemia Associated With Near-Tetraploid Karyotype and Mutations in the FLT3 Gene;Laboratory Medicine;2011-09
4. Single institute study of FLT3 mutation in acute myeloid leukemia with near tetraploidy in Serbia;Journal of Genetics;2009-06-09
5. Importance of early detection and follow-up of FLT3 mutations in patients with acute myeloid leukemia;Annals of Hematology;2007-06-20
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