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Article

Linkage analyses of chromosomal region 18p11-q12 in dyslexia.

Journal of neural transmission (Vienna, Austria : 1996) - 1 Mar 2006

Schumacher J, König I R, Plume E, Propping P, Warnke A, Manthey M, Duell M, Kleensang A, Repsilber D, Preis M, Remschmidt H, Ziegler A, Nöthen M M, Schulte-Körne G

Abstract excerpt

Dyslexia is characterized as a significant impairment in reading and spelling ability that cannot be explained by low intelligence, low school attendance or deficits in sensory acuity. It is known to be a hereditary disorder that affects about 5% of school aged children, making it the most common of childhood learning disorders. Several susceptibility loci have been reported on chromosomes 1, 2, 3, 6, 15, and 18....

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Identifiers

PMID: 16075186
DOI: 10.1007/s00702-005-0336-y

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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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Linkage analyses of chromosomal region 18p11-q12 in dyslexia.PMID 16075186Read ↗

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Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.Semantic proximity Read ↗

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