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

Copy neutral loss of heterozygosity in 20q in chronic lymphocytic leukemia/small lymphocytic lymphoma.

Cancer genetics - 1 Mar 2014

Pei Jianming, Robu Valentin, Feder Madelyn, Cheung Mitchell, Neumann-Domer Erin, Talarchek Jacqueline, Dulaimi Essel, Millenson Michael M, Testa Joseph R

Abstract excerpt

Single nucleotide polymorphism (SNP)-based chromosome microarray analysis was used to uncover copy neutral loss of heterozygosity (LOH) in the long arm of chromosome 20 in blood or bone marrow specimens from three patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). Al...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 20
Share to ASXL1 gene
Share to Heterozygote

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukemia, Lymphocytic, Chronic, B-Cell

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 24704113
DOI: 10.1016/j.cancergen.2014.02.005
PMCID: PMC4010307

Genes

ASXL1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24704113-2026-09-04.2. 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 · 9 closest

Copy neutral loss of heterozygosity in 20q in chronic lymphocytic leukemia/small lymphocytic lymphoma.PMID 24704113Read ↗

Characterization of chromosome arm 20q abnormalities in myeloid malignancies using genome-wide single nucleotide polymorphism array analysis.Semantic proximity Read ↗

Single nucleotide polymorphism array-based karyotyping shows sequential genomic changes from monosomy to copy-neutral loss of heterozygosity of chromosome 7 and 20q deletion within a balanced translocation t(14;20) in AML.Semantic proximity Read ↗

Differences between chronic lymphocytic leukaemia and small lymphocytic lymphoma cells by proteomic profiling and SNP microarray analysis.Semantic proximity Read ↗

Evaluation of 13q14 status in patients with chronic lymphocytic leukemia using single nucleotide polymorphism-based techniques.Semantic proximity Read ↗

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

Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays.Semantic proximity Read ↗

MicroRNA losses in the frequently deleted region of 7q in SMZLSemantic proximity Read ↗

Disparate expression of the <i>PTEN</i> gene: a novel finding in B‐cell chronic lymphocytic leukaemia (B‐CLL)Semantic proximity Read ↗

Recurrent allelic deletions of chromosome arms 15q and 16q in human small cell lung carcinomas.Semantic proximity Read ↗

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