Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17.
about
Linguistic tone is related to the population frequency of the adaptive haplogroups of two brain size genes, ASPM and MicrocephalinDyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sampleEtiology and neuropsychology of comorbidity between RD and ADHD: the case for multiple-deficit modelsDyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutationGenetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficitsThe genetics of reading disabilities: from phenotypes to candidate genesGenome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colorsIdentification of candidate genes for dyslexia susceptibility on chromosome 18.Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.A theoretical molecular network for dyslexia: integrating available genetic findings.Genome-wide screening for DNA variants associated with reading and language traitsGenome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localization.In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.Linkage analysis in a Dutch population isolate shows no major gene for left-handedness or atypical language lateralizationMotor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family.Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.Meeting the Challenges of Neuroimaging Genetics.Molecular genetics of dyslexia: an overview.Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319.Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p.Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families.Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.Familial dyslexia in a large Swedish family: a whole genome linkage scan.SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample.SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.Current Genetic Discoveries and Education: Strengths, Opportunities, and LimitationsA Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1
P2860
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P2860
Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17.
description
2006 nî lūn-bûn
@nan
2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Replication of reported linkag ...... gions on chromosomes 4 and 17.
@ast
Replication of reported linkag ...... gions on chromosomes 4 and 17.
@en
Replication of reported linkag ...... gions on chromosomes 4 and 17.
@nl
type
label
Replication of reported linkag ...... gions on chromosomes 4 and 17.
@ast
Replication of reported linkag ...... gions on chromosomes 4 and 17.
@en
Replication of reported linkag ...... gions on chromosomes 4 and 17.
@nl
prefLabel
Replication of reported linkag ...... gions on chromosomes 4 and 17.
@ast
Replication of reported linkag ...... gions on chromosomes 4 and 17.
@en
Replication of reported linkag ...... gions on chromosomes 4 and 17.
@nl
P2860
P50
P356
P1476
Replication of reported linkag ...... gions on chromosomes 4 and 17.
@en
P2093
Michelle Luciano
P2860
P2888
P304
P356
10.1038/SJ.EJHG.5201739
P577
2006-11-22T00:00:00Z