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Article

Single nucleotide polymorphism array-based karyotyping in acute myeloid leukemia or myelodysplastic syndrome with trisomy 8 as the sole chromosomal abnormality.

Acta haematologica - 1 Jan 2013

Hahm Chorong, Mun Yeung Chul, Seong Chu Myong, Han Sung-Hee, Chung Wha Soon, Huh Jungwon

Abstract excerpt

The clinical heterogeneity of patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) with trisomy 8 as the sole abnormality may result from cytogenetically undetectable genetic changes. The purpose of this study was to identify hidden genomic aberrations not detected by metaphase cytogenetics (MC) using high-resolution single nucleotide polymorphism array (SNP-A)-based karyotyping in AML/MDS...

Read the complete abstract on PubMed

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Share to Abnormal Karyotype
Share to Aged, 80 and over

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 8

Share to Leukemia, Myeloid, Acute

Share to Loss of Heterozygosity

Share to Myelodysplastic Syndromes

Share to Polymorphism, Single Nucleotide

Share to Trisomy

Source

Identifiers

PMID: 23208021
DOI: 10.1159/000343420

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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