Dyslexia is a common, complex disorder, which is thought to have a genetic component.
There have been numerous reports of linkage to several regions of the genome for dyslexia …

Dyslexia is a common heterogeneous disorder with a significant genetic component.
Multiple studies have replicated the evidence for linkage between variously defined …

Dyslexia is a common and genetically complex trait that manifests primarily as a reading
disability independent of general intelligence and educational opportunity. Strong evidence …

A linkage study of 96 dyslexia families containing at least two affected siblings (totaling 877
individuals) has found evidence for a dyslexia susceptibility gene on chromosome 6q11. 2 …

In this study, we attempted to confirm genetic linkage to developmental dyslexia and reading‐
related quantitative traits of loci that have been shown to be associated with dyslexia in …

According to the data published by US Department of Education [1999], about 30% of US
fourth-grade students read below their expected grade level. Moreover, the reading skills of …

Dyslexia is a common learning disability exhibited as a delay in acquiring reading skills
despite adequate intelligence and instruction. Reading single real words (real‐word …

A locus on chromosome 2p12-16 has been implicated in dyslexia susceptibility by two
independent linkage studies, including our own study of 119 nuclear twin-based families …

Analysis of genetic linkage to dyslexia was performed using 133,165 array‐based SNPs
genotyped in 718 persons from 101 dyslexia‐affected families. Results showed five linkage …

To understand the genetic architecture of dyslexia and identify the locations of genes
involved, we performed linkage analyses in multigenerational families using a phonological …