about
Comorbidity of ADHD and dyslexia.Dyslexia and familial high blood pressure: an observational pilot studyPleiotropic functions of EAPII/TTRAP/TDP2: cancer development, chemoresistance and beyondSame or different? Insights into the etiology of phonological awareness and rapid naming.A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.Gray matter heritability in family-based and population-based studies using voxel-based morphometry.The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilitiesAssociation of reading disabilities with regions marked by acetylated H3 histones in KIAA0319.Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects.Sensory, cognitive, and linguistic factors in the early academic performance of elementary school children: The Benton-IU project.
P2860
Q34132050-03DC983A-C9F9-4D4A-A2E0-AC618784A2BEQ35272108-CC7F7A7C-1C2A-45DA-A32C-50952B644A8DQ35600743-FD81A3AD-8EED-4E44-827B-9823DB42E73DQ37257443-0EF31E08-41D1-4124-B3FA-DC28E56E8141Q37738889-4F9EB03E-A129-4CE9-A97F-958EFA25C19DQ38987624-0A4FE500-2B95-400A-BCF9-1271ABF90B52Q42219905-17ABC8FE-1282-473F-8E5F-828CBFFDD590Q42292717-16892FF8-F0D3-4DCC-8C58-1BA0E7A2C7B1Q42613559-FBDB2A59-49E2-4723-9932-442B9FF0DBBEQ50477199-BE1EBC9F-A23A-4FC2-AE37-A549CA3FD88A
P2860
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Reading disability: evidence for a genetic etiology.
@ast
Reading disability: evidence for a genetic etiology.
@en
type
label
Reading disability: evidence for a genetic etiology.
@ast
Reading disability: evidence for a genetic etiology.
@en
prefLabel
Reading disability: evidence for a genetic etiology.
@ast
Reading disability: evidence for a genetic etiology.
@en
P356
P1476
Reading disability: evidence for a genetic etiology.
@en
P2093
P2860
P2888
P356
10.1007/PL00010695
P478
P577
1999-01-01T00:00:00Z