The dyslexia susceptibility locus DYX2 (chr. 6p21-p22) harbours two candidate genes, DCDC2 and KIAA0319. In 2006, Harold et al. reported evidence for interaction between both genes. Having previously identified a risk haplotype for dyslexia in DCDC2, but not KIAA0319, in German families, we also tested for interaction between this risk haplotype and KIAA0319. We found a nominally significant association for the quantitative dimension "word reading", the core phenotype in the study of Harold et al., which may be considered as supportive evidence
p>Developmental dyslexia, also known as specific reading disability, is characterized by persistent ...
We searched for linkage disequilibrium (LD) in 137 triads with dyslexia, using markers that span the...
International audience: Dyslexia is one of the most common childhood disorders with a prevalence of ...
The dyslexia susceptibility locus DYX2 (chr. 6p21-p22) harbours two candidate genes, DCDC2 and KIAA0...
The DYX2 locus on chromosome 6p22.2 is the most replicated region of linkage to developmental dyslex...
Dyslexia is one of the most common childhood disorders with a prevalence of around 5-10% in school-a...
Linkage between developmental dyslexia (DD) and chromosome 6p has been replicated in a number of ind...
Linkage between developmental dyslexia (DD) and chromosome 6p has been replicated in a number of ind...
Objective(S): Developmental dyslexia is a heritable condition, with genetic factors accounting for 4...
A locus on chromosome 1p34-36 (DYX8) has been linked to developmental dyslexia or reading disabiliti...
Reading disability (RD) and language impairment (LI) are common neurodevelopmental disorders with mo...
We searched for linkage disequilibrium (LD) in 137 triads with dyslexia, using markers that span the...
Dyslexia is a complex reading and writing disorder with a strong genetic component. In a German case...
Developmental dyslexia (DD) is a heritable, complex genetic disorder associated with impairment in r...
p>Developmental dyslexia, also known as specific reading disability, is characterized by persistent ...
We searched for linkage disequilibrium (LD) in 137 triads with dyslexia, using markers that span the...
International audience: Dyslexia is one of the most common childhood disorders with a prevalence of ...
The dyslexia susceptibility locus DYX2 (chr. 6p21-p22) harbours two candidate genes, DCDC2 and KIAA0...
The DYX2 locus on chromosome 6p22.2 is the most replicated region of linkage to developmental dyslex...
Dyslexia is one of the most common childhood disorders with a prevalence of around 5-10% in school-a...
Linkage between developmental dyslexia (DD) and chromosome 6p has been replicated in a number of ind...
Linkage between developmental dyslexia (DD) and chromosome 6p has been replicated in a number of ind...
Objective(S): Developmental dyslexia is a heritable condition, with genetic factors accounting for 4...
A locus on chromosome 1p34-36 (DYX8) has been linked to developmental dyslexia or reading disabiliti...
Reading disability (RD) and language impairment (LI) are common neurodevelopmental disorders with mo...
We searched for linkage disequilibrium (LD) in 137 triads with dyslexia, using markers that span the...
Dyslexia is a complex reading and writing disorder with a strong genetic component. In a German case...
Developmental dyslexia (DD) is a heritable, complex genetic disorder associated with impairment in r...
p>Developmental dyslexia, also known as specific reading disability, is characterized by persistent ...
We searched for linkage disequilibrium (LD) in 137 triads with dyslexia, using markers that span the...
International audience: Dyslexia is one of the most common childhood disorders with a prevalence of ...