Quantitative Whole Genome Analysis of Sequential Samples From Patients with B CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B Cell Transcription Factors
Main Authors: | Timbs, A, Knight, S, SadighiAkha, E, Burns, A, Dreau, H, Hewitt, A, Hatton, C, Yau, C, Holmes, C, Taylor, J, Schuh, A |
---|---|
Format: | Conference item |
Published: |
2010
|
Similar Items
-
Quantitative Whole Genome Analysis of Sequential Samples From Patients with B-CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B-Cell Transcription Factors
by: Timbs, A, et al.
Published: (2010) -
Identification of Novel Recurrent Copy Number Variations and Regions of Copy-Neutral Loss of Heterozygosity by High Resolution Genomic Array in Pre-Treatment and Relapsed B-CLL.
by: Knight, S, et al.
Published: (2009) -
IDENTIFICATION OF NOVEL RECURRENT COPY NUMBER VARIATIONS BY HIGH RESOLUTION COMPARATIVE GENOME HYBRIDISATION
by: Schuh, A, et al.
Published: (2009) -
Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemia.
by: Knight, S, et al.
Published: (2012) -
Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemia.
by: Knight, S, et al.
Published: (2012)