Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Del(20q) in patients with chronic lymphocytic leukemia: a therapy-related abnormality involving lymphoid or myeloid cells.

Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc - 1 Aug 2015

Yin C Cameron, Tang Guilin, Lu Gary, Feng Xiaoli, Keating Michael J, Medeiros L Jeffrey, Abruzzo Lynne V

Abstract excerpt

Deletion 20q (Del(20q)), a common cytogenetic abnormality in myeloid neoplasms, is rare in chronic lymphocytic leukemia. We report 64 patients with chronic lymphocytic leukemia and del(20q), as the sole abnormality in 40, a stemline abnormality in 21, and a secondary abnormality in 3 cases. Fluor...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 20

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Immunoglobulin Heavy Chain

Share to Immunoglobulin Variable Region

Share to Immunophenotyping

Share to Leukemia, Lymphocytic, Chronic, B-Cell

Share to Lymphocytes

Share to Myeloid Cells

Source

Open in PubMed Open full text

Identifiers

PMID: 25953391
DOI: 10.1038/modpathol.2015.58
PMCID: PMC4522203

Genes

ZAP70

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25953391-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Del(20q) in patients with chronic lymphocytic leukemia: a therapy-related abnormality involving lymphoid or myeloid cells.PMID 25953391Read ↗

Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20.Semantic proximity Read ↗

Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regionsSemantic proximity Read ↗

Hematologic Disorders Associated With Deletions of Chromosome 20q:A Clinicopathologic Study of 107 PatientsSemantic proximity Read ↗

Chronic lymphocytic leukemia with t(14;18)(q32;q21).Semantic proximity Read ↗

Genomic Aberrations and Survival in Chronic Lymphocytic LeukemiaSemantic proximity Read ↗

Refinement of the commonly deleted segment in myeloid leukemias with a del(20q).Semantic proximity Read ↗

The complex karyotype and chronic lymphocytic leukemia: prognostic value and diagnostic recommendationsSemantic proximity Read ↗

Chronic lymphocytic leukemia with t(14;19)(q32;q13) is characterized by atypical morphologic and immunophenotypic features and distinctive genetic features.Semantic proximity Read ↗

DELETIONS OF CHROMOSOME 20q AND THE PATHOGENESIS OF MYELOPROLIFERATIVE DISORDERSSemantic proximity Read ↗

Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genesSemantic proximity Read ↗

Chromosome aberrations detected by conventional karyotyping using novel mitogens in chronic lymphocytic leukemia with “normal” FISH: correlations with clinicobiologic parametersSemantic proximity Read ↗

Dic(17;18)(p11.2;p11.2) is a recurring abnormality in chronic lymphocytic leukaemia associated with aggressive disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.