Clinical use of SNP-microarrays for the detection of genome-wide changes in haematological malignancies
Author:
Publisher
Elsevier BV
Subject
Oncology,Hematology
Reference168 articles.
1. Chromothripsis Is a recurrent genomic abnormality in High-risk myelodysplastic syndromes;Abáigar;PLOS ONE,2016
2. Practice guidelines for Genetic/Genomic testing in pediatric B-lineage acute lymphoblastic leukemia (B-ALL): a cancer genomics consortium (CGC) workgroup;Akkari;Cancer Genetics,2017
3. 19. Evidence-based review of genomic aberrations in T-ALL: strategy and progress of CGC T-ALL working group;Akkari;Cancer Genetics,2018
4. Gene amplification in cancer;Albertson;Trends in Genetics,2006
5. Amplification of c-MYC and MLL genes as a marker of clonal cell progression in patients with myeloid malignancy and trisomy of chromosomes 8 or 11;Angelova;Balkan J. Medical Genetics : BJMG,2011
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