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Article

Significant linkage at chromosome 19q for otitis media with effusion and/or recurrent otitis media (COME/ROM).

BMC medical genetics - 26 Sept 2011

Chen Wei-Min, Allen E Kaitlynn, Mychaleckyj Josyf C, Chen Fang, Hou Xuanlin, Rich Stephen S, Daly Kathleen A, Sale Michèle M

Abstract excerpt

BACKGROUND: In previous analyses, we identified a region of chromosome 19 as harboring a susceptibility locus for chronic otitis media with effusion and/or recurrent otitis media (COME/ROM). Our aim was to further localize the linkage signal and ultimately identify the causative variant or variants. We followed up our previous linkage scan with dense SNP genotyping across in a 5 Mb region. A total of 607...

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Share to Chromosomes, Human, Pair 19
Share to Genetic Linkage

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Linkage Disequilibrium

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Share to Polymorphism, Single Nucleotide

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Source

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Identifiers

PMID: 21943191
DOI: 10.1186/1471-2350-12-124
PMCID: PMC3191346

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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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