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

Oligonucleotide array-CGH reveals cryptic gene copy number alterations in karyotypically normal acute myeloid leukemia

1 Feb 2007

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Acute Myeloid Leukemia Research
Share to Cancer Genomics and Diagnostics
Share to Genomic variations and chromosomal abnormalities

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 17268525
DOI: 10.1038/sj.leu.2404543

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Oligonucleotide array-CGH reveals cryptic gene copy number alterations in karyotypically normal acute myeloid leukemiaPMID 17268525Read ↗

Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevanceSemantic proximity Read ↗

Genomic analysis of acute myeloid leukemia: potential for new prognostic indicators.Semantic proximity Read ↗

Array CGH in human leukemia: from somatics to genetics.Semantic proximity Read ↗

Genome-wide arrays in routine diagnostics of hematological malignancies.Semantic proximity Read ↗

Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridizationSemantic proximity Read ↗

Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype.Semantic proximity Read ↗

Array comparative genomic hybridization analysis of adult acute leukemia patients.Semantic proximity Read ↗

Array comparative genomic hybridization of peripheral blood granulocytes of patients with myelodysplastic syndrome detects karyotypic abnormalities.Semantic proximity Read ↗

Detection of copy number alterations in acute myeloid leukemia and myelodysplastic syndromes.Semantic proximity Read ↗

Gene expression patterns in acute myeloid leukemia correlate with centrosome aberrations and numerical chromosome changesSemantic proximity Read ↗

Detection of DNA copy number alterations in cancer by array comparative genomic hybridizationSemantic proximity Read ↗

Microarray-based comparative genomic hybridization of cancer targets reveals novel, recurrent genetic aberrations in the myelodysplastic syndromesSemantic proximity Read ↗

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