All Stories

  1. Acute promyelocytic leukemia with del(6)(p22) and atypical bcr2 PML::RARA fusion transcript: a case report
  2. Concomitant JAK2 V617F mutation and rare e1a2 BCR-ABL1 transcript isoform in a patient with Myeloproliferative Neoplasm
  3. BCR/ABL1 fluorescence in situ hybridization fusion signals on both copies of chromosome 22 in a Philadelphia-masked chronic myeloid leukemia case: implication for the therapy
  4. A double-hit High-grade B-cell lymphoma with three-way translocation t(3;8;14)(q27;q24;q32) involving BCL6, MYC, and IGH
  5. A Case of Blastic Plasmacytoid Dendritic Cell Neoplasm Extensively Studied by Flow Cytometry and Immunohistochemistry
  6. microwave-assisted fluorescence in situ hybridization
  7. Chlorambucil plus rituximab with or without maintenance rituximab as first-line treatment for elderly chronic lymphocytic leukemia patients
  8. P-067 The effectiveness of FISH technique for the detection of the cryptic chromosomal aberration in patients with suspicion of MDS
  9. Erythroleukemia presenting with myeloid sarcoma of the lung as detected by immunophenotypic analysis of bronchoalveolar lavage fluid
  10. Rituximab Plus Chlorambucil As Initial Treatment for Elderly Patients with Chronic Lymphocytic Leukemia (CLL): Effect of Pre-Treatment Biological Characteristics and Gene Expression Patterns on Response to Treatment
  11. Three copies of isochromosome 8q in Ph+ B-cell acute lymphoblastic leukemia
  12. Double supernumerary isochromosome 4p in acute myelomonocytic leukemia
  13. A Phase II Study of Chlorambucil Plus Rituximab Followed by Maintenance Versus Observation In Elderly Patients with Previously Untreated Chronic Lymphocytic Leukemia: Results of the First Interim Analysis
  14. PML/RAR-α fusion transcript and polyploidy in acute promyelocytic leukemia without t(15;17)
  15. A Novel Mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 disease Communicated by: Haig H. Kazazian Online Citation: Human Mutation, Mutation in Brief #269(1999) Online http://journals.wiley.com/1...
  16. A Novel Mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 disease
  17. Congenital hypomyelination due to myelin protein zero Q215X mutation
  18. Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type II
  19. Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type II