Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease
S Branford, P Wang, DT Yeung… - Blood, The Journal …, 2018 - ashpublications.org
Genomic events associated with poor outcome in chronic myeloid leukemia (CML) are
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease
S Branford, P Wang, DT Yeung, D Thomson… - …, 2018 - pubmed.ncbi.nlm.nih.gov
Genomic events associated with poor outcome in chronic myeloid leukemia (CML) are
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease.
S Branford, P Wang, DT Yeung, D Thomson, A Purins… - Blood, 2018 - europepmc.org
Genomic events associated with poor outcome in chronic myeloid leukemia (CML) are
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
[HTML][HTML] Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease
S Branford, P Wang, DT Yeung, D Thomson, A Purins… - Blood, 2018 - Elsevier
Genomic events associated with poor outcome in chronic myeloid leukemia (CML) are
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease
S Branford, P Wang, DT Yeung, D Thomson, A Purins… - Blood, 2018 - cir.nii.ac.jp
抄録< jats: title> Key Points</jats: title>< jats: p> Next-generation sequencing revealed
variants in cancer-associated genes at diagnosis of CML more frequently in patients with …
variants in cancer-associated genes at diagnosis of CML more frequently in patients with …
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease
S Branford, P Wang, DT Yeung, D Thomson… - 2018 - digital.library.adelaide.edu.au
Genomic events associated with poor outcome in chronic myeloid leukemia (CML) are
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease
S Branford, P Wang, D Yeung, D Thomson… - …, 2018 - researchnow.flinders.edu.au
Genomic events associated with poor outcome in chronic myeloid leukemia (CML) are
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease
S Branford, P Wang, D Yeung, D Thomson… - Blood, 2018 - research.sahmri.org.au
Genomic events associated with poor outcome in chronic myeloid leukemia (CML) are
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease
S Branford, P Wang, DT Yeung, D Thomson… - 2018 - hekyll.services.adelaide.edu.au
Genomic events associated with poor outcome in chronic myeloid leukemia (CML) are
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …
poorly understood. We performed whole-exome sequencing, copy-number variation, and/or …