Confirmation of a dyslexia susceptibility locus on chromosome 1p34-p36 in a set of 100 Canadian families
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Genetics of dyslexia: the evolving landscapeStrong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.Association of short-term memory with a variant within DYX1C1 in developmental dyslexiaThe complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexiaGenome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colorsConverging evidence for triple word form theory in children with dyslexia.Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.A theoretical molecular network for dyslexia: integrating available genetic findings.Are there susceptibility factors for primary progressive aphasia?The 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.Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settingsAssociation of the ROBO1 gene with reading disabilities in a family-based analysis.Embryonic disruption of the candidate dyslexia susceptibility gene homolog Kiaa0319-like results in neuronal migration disorders.Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.Molecular genetics of dyslexia: an overview.Non-nuclear Pool of Splicing Factor SFPQ Regulates Axonal Transcripts Required for Normal Motor Development.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.[Phonological awareness, working memory, reading and writing performances in familial dyslexia].Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.Molecular genetics and molecular biology of dyslexia.Further evidence of pleiotropy influencing speech and language: analysis of the DYX8 region.Linkage of speech sound disorder to reading disability loci.A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic lociA Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1Systematic re-examination of carriers of balanced reciprocal translocations: a strategy to search for candidate regions for common and complex diseases
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Confirmation of a dyslexia susceptibility locus on chromosome 1p34-p36 in a set of 100 Canadian families
description
article
@en
im Jahr 2004 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована у 2004
@uk
name
Confirmation of a dyslexia sus ...... a set of 100 Canadian families
@en
Confirmation of a dyslexia sus ...... a set of 100 Canadian families
@nl
type
label
Confirmation of a dyslexia sus ...... a set of 100 Canadian families
@en
Confirmation of a dyslexia sus ...... a set of 100 Canadian families
@nl
prefLabel
Confirmation of a dyslexia sus ...... a set of 100 Canadian families
@en
Confirmation of a dyslexia sus ...... a set of 100 Canadian families
@nl
P2093
P356
P1476
Confirmation of a dyslexia sus ...... a set of 100 Canadian families
@en
P2093
Bonnie J. Kaplan
Jordana Tzenova
L. Leigh Field
Tracey L. Petryshen
P304
P356
10.1002/AJMG.B.20139
P577
2004-01-01T00:00:00Z