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Article

Genome-wide high-resolution screening in Dupuytren's disease reveals common regions of DNA copy number alterations.

The Journal of hand surgery - 1 Jul 2010

Shih Barbara B, Tassabehji May, Watson James S, McGrouther Angus D, Bayat Ardeshir

Abstract excerpt

PURPOSE: Dupuytren's disease (DD) is a familial disorder with a high genetic susceptibility in white people; however, its etiopathogenesis remains unknown. Previous comparative genomic hybridization studies using lower-resolution, 44-k oligonucleotide-based arrays revealed no copy number variation (CNV) changes in DD. In this study, we used a higher-resolution genome-wide screening (next-generation microarrays)...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 20561756
DOI: 10.1016/j.jhsa.2010.03.006

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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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