Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.

American journal of human genetics - 1 Nov 1998

Field L L, Kaplan B J

Abstract excerpt

Previous studies have suggested that a locus predisposing to specific reading disability (dyslexia) resides on chromosome 6p23-p21.3. We investigated 79 families having at least two siblings affected with phonological coding dyslexia, the most common form of reading disability (617 people genotyped, 294 affected), and we tested for linkage with the genetic markers reported to be linked to dyslexia in those...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to White People
Share to Alleles
Share to Child

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

Share to Chromosome Mapping

Share to Gene Frequency

Share to Genetic Linkage

Share to Genetic Markers

Share to Genotype

Source

Open in PubMed Open full text

Identifiers

PMID: 9792873
DOI: 10.1086/302107
PMCID: PMC1377556

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.PMID 9792873Read ↗

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 ↗

Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia.Semantic proximity Read ↗

Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection.Semantic proximity Read ↗

Continuing the search for dyslexia genes on 6p.Semantic proximity Read ↗

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

Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation.Semantic proximity Read ↗

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia.Semantic proximity Read ↗

Linkage analyses of chromosomal region 18p11-q12 in dyslexia.Semantic proximity Read ↗

A major susceptibility locus for specific language impairment is located on 13q21.Semantic proximity Read ↗

Evidence for linkage and association with reading disability on 6p21.3-22.Semantic proximity Read ↗

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

Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair design.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.