A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32
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A multi-platform draft de novo genome assembly and comparative analysis for the Scarlet Macaw (Ara macao)The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexiaGenetics of dyslexia: the evolving landscapeAltered ultrasonic vocalization in mice with a disruption in the Foxp2 geneIdentification of FOXP2 truncation as a novel cause of developmental speech and language deficitsStrong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing childrenFamily-based association study of DYX1C1 variants in autismAssociation of short-term memory with a variant within DYX1C1 in developmental dyslexiaImaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.The genetics of reading disabilities: from phenotypes to candidate genesThe aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and languageGenome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colorsCharacterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQConverging evidence for triple word form theory in children with dyslexia.Identification of candidate genes for dyslexia susceptibility on chromosome 18.Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading.Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.A theoretical molecular network for dyslexia: integrating available genetic findings.Inter-relationships among behavioral markers, genes, brain and treatment in dyslexia and dysgraphiaGenome-wide screening for DNA variants associated with reading and language traitsExamination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairmentThe genetics of developmental dyslexia.Genome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localization.Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17.In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch familyLanguage impairment and dyslexia genes influence language skills in children with autism spectrum disorders.Imaging genetics of FOXP2 in dyslexia.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.Science and society: applications of behavioural genetics: outpacing the science?Genetic studies of stuttering in a founder populationLanguage Impairment Resulting from a de novo Deletion of 7q32.1q33.Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.Molecular genetics of dyslexia: an overview.Identification of NCAN as a candidate gene for developmental dyslexia.Approach to epigenetic analysis in language disordersAssociation of reading disabilities with regions marked by acetylated H3 histones in KIAA0319.Reply to Ray and Weeks: Linkage for Restless Legs Syndrome on Chromosome 9p Is Significant.
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P2860
A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32
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2003 nî lūn-bûn
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2003 թուականի Մայիսին հրատարակուած գիտական յօդուած
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2003 թվականի մայիսին հրատարակված գիտական հոդված
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2003年の論文
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2003年論文
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2003年論文
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2003年論文
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2003年論文
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2003年論文
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2003年论文
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name
A genome scan for developmenta ...... d suggests a new locus on 7q32
@ast
A genome scan for developmenta ...... d suggests a new locus on 7q32
@en
type
label
A genome scan for developmenta ...... d suggests a new locus on 7q32
@ast
A genome scan for developmenta ...... d suggests a new locus on 7q32
@en
prefLabel
A genome scan for developmenta ...... d suggests a new locus on 7q32
@ast
A genome scan for developmenta ...... d suggests a new locus on 7q32
@en
P2093
P356
P1476
A genome scan for developmenta ...... d suggests a new locus on 7q32
@en
P2093
Hannula-Jouppi K
Kaaranen M
Lyytinen H
Myllyluoma B
Nopola-Hemmi J
Voutilainen A
P304
P356
10.1136/JMG.40.5.340
P407
P50
P577
2003-05-01T00:00:00Z