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Article

Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15.

American journal of human genetics - 1 Jan 1997

Grigorenko E L, Wood F B, Meyer M S, Hart L A, Speed W C, Shuster A, Pauls D L

Abstract excerpt

Six extended dyslexic families with at least four affected individuals were genotyped with markers in three chromosomal regions: 6p23-p21.3, 15pter-qter, and 16pter-qter. Five theoretically derived phenotypes were used in the linkage analyses: (1) phonological awareness; (2) phonological decoding...

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Identifiers

PMID: 8981944
PMCID: PMC1712535

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-8981944-2026-09-02.1. Manifest publication-graph-cohort-2026-09-02.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15.PMID 8981944Read ↗

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Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.Semantic proximity Read ↗

A multidisciplinary approach to understanding developmental dyslexia within working-memory architecture: genotypes, phenotypes, brain, and instruction.Semantic proximity Read ↗

Absence of significant linkage between phonological coding dyslexia and chromosome 6p23-21.3, as determined by use of quantitative-trait methods: confirmation of qualitative analyses.Semantic proximity Read ↗

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