From cryptic chromosomal lesions to pathologically relevant genes: Integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype
Author:
Publisher
Wiley
Subject
Cancer Research,Genetics
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1. Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms;Cancer Genetics;2018-12
2. Relationship between Altered miRNA Expression and DNA Methylation of the DLK1-DIO3 Region in Azacitidine-Treated Patients with Myelodysplastic Syndromes and Acute Myeloid Leukemia with Myelodysplasia-Related Changes;Cells;2018-09-14
3. Impact of copy neutral loss of heterozygosity and total genome aberrations on survival in myelodysplastic syndrome;Modern Pathology;2017-12-15
4. Identify latent chromosomal aberrations relevant to myelodysplastic syndromes;Scientific Reports;2017-09-04
5. Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes;PLOS ONE;2016-10-14
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