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Article

Targeted resequencing of 9p in acute lymphoblastic leukemia yields concordant results with array CGH and reveals novel genomic alterations.

Genomics - 1 Sept 2013

Sarhadi Virinder Kaur, Lahti Leo, Scheinin Ilari, Tyybäkinoja Anne, Savola Suvi, Usvasalo Anu, Räty Riikka, Elonen Erkki, Ellonen Pekka, Saarinen-Pihkala Ulla M, Knuutila Sakari

Abstract excerpt

Genetic alterations of the short arm of chromosome 9 are frequent in acute lymphoblastic leukemia. We performed targeted sequencing of 9p region in 35 adolescent and adult acute lymphoblastic leukemia patients and sought to investigate the sensitivity of detecting copy number alterations in comparison with array comparative genomic hybridization (aCGH), and besides, to detect novel genetic anomalies. We found a...

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Share to Chromosome Aberrations
Share to Chromosomes, Human, Pair 9

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Comparative Genomic Hybridization

Share to DNA Copy Number Variations

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Share to Precursor Cell Lymphoblastic Leukemia-Lymphoma

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Identifiers

PMID: 23333812
DOI: 10.1016/j.ygeno.2013.01.001

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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