Pages that link to "Q39280199"

The following pages link to Identification of unbalanced genome copy number abnormalities in patients with multiple myeloma by single-nucleotide polymorphism genotyping microarray analysis. (Q39280199):

Displaying 11 items.

• The Basic Biology of PP2A in Hematologic Cells and Malignancies (Q28088697) (← links)
• Jumping translocations of 1q12 in multiple myeloma: a novel mechanism for deletion of 17p in cytogenetically defined high-risk disease (Q37709342) (← links)
• Role of non-HLA gene polymorphisms in graft-versus-host disease. (Q38129337) (← links)
• SNP Array in Hematopoietic Neoplasms: A Review (Q38947537) (← links)
• Novel recurrent chromosomal aberrations detected in clonal plasma cells of light chain amyloidosis patients show potential adverse prognostic effect: first results from a genome-wide copy number array analysis (Q40274316) (← links)
• Widespread genetic heterogeneity in multiple myeloma: implications for targeted therapy (Q43024864) (← links)
• Challenges and Promises of Genetic Stratification of Risk in Multiple Myeloma (Q50319298) (← links)
• Progress in the identification of gene mutations involved in multiple myeloma. (Q64898357) (← links)
• Guidelines for genomic array analysis in acquired haematological neoplastic disorders (Q87092957) (← links)
• Can genome array screening replace FISH as a front-line test in multiple myeloma? (Q87733927) (← links)
• Three-dimensional genome: developmental technologies and applications in precision medicine (Q90170774) (← links)