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

Prognostic impact of chromosomal aberrations in Ewing tumours

1 Jun 2002

Abstract excerpt

Although greater than 50% of Ewing tumours contain non-random cytogenetic aberrations in addition to the pathognomonic 22q12 rearrangements, little is known about their prognostic significance. To address this question, tumour samples from 134 Ewing tumour patients were analysed using a combination of classical cytogenetics, comparative genomic and fluorescence in situ hybridisation. The evaluation of the...

Read the complete abstract on PubMed

Topics

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

Share to Cardiac tumors and thrombi
Share to Lymphoma Diagnosis and Treatment
Share to Sarcoma Diagnosis and Treatment

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 12087464
DOI: 10.1038/sj.bjc.6600332

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prognostic impact of chromosomal aberrations in Ewing tumoursPMID 12087464Read ↗

Genetic imbalances revealed by comparative genomic hybridization in Ewing tumorsSemantic proximity Read ↗

Recurrent gains of 1q, 8 and 12 in the Ewing family of tumours by comparative genomic hybridizationSemantic proximity Read ↗

Ewing’s sarcoma: diagnostic, prognostic, and therapeutic implications of molecular abnormalitiesSemantic proximity Read ↗

Ploidy and karyotype complexity are powerful prognostic indicators in the Ewing's sarcoma family of tumors: A study by the United Kingdom Cancer Cytogenetics and the Children's Cancer and Leukaemia GroupSemantic proximity Read ↗

Frequency and Implications of Chromosome 8 and 12 Gains in Ewing SarcomaSemantic proximity Read ↗

Combined use of expression and CGH arrays pinpoints novel candidate genes in Ewing sarcoma family of tumorsSemantic proximity Read ↗

Additional chromosome 1q aberrations and der(16)t(1;16), correlation to the phenotypic expression and clinical behavior of the Ewing family of tumors.Semantic proximity Read ↗

Genomic imbalances detected by comparative genomic hybridization are prognostic markers in invasive ductal breast carcinomasSemantic proximity Read ↗

Chromosome 9p21 gene copy number and prognostic significance of p16 in ESFTSemantic proximity Read ↗

Diagnostic value of the molecular genetic detection of the t(11;22) translocation in Ewing's tumoursSemantic proximity Read ↗

Prognostic impact of INK4A deletion in Ewing sarcomaSemantic proximity Read ↗

Different patterns of chromosomal imbalances in metastasising and non-metastasising primary breast carcinomas.Semantic proximity Read ↗

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