TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort. - Wikidata - awgldk - TriplyDB

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

http://www.wikidata.org/entity/Q52040525

about

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia Genetics of dyslexia: the evolving landscape DYX1C1 is required for axonemal dynein assembly and ciliary motility DCDC2, KIAA0319 and CMIP are associated with reading-related traits The human lexinome: genes of language and reading Genetic factors contributing to human primary ciliary dyskinesia and male infertility Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation Association of short-term memory with a variant within DYX1C1 in developmental dyslexia Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits Deficits in learning and memory in mice with a mutation of the candidate dyslexia susceptibility gene Dyx1c1 Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.Tackling the 'dyslexia paradox': reading brain and behavior for early markers of developmental dyslexiax.The genetics of reading disabilities: from phenotypes to candidate genes Progress towards a cellular neurobiology of reading disability.Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.An informatics approach to integrating genetic and neurological data in speech and language neuroscience.The rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation.Understanding the complex etiologies of developmental disorders: behavioral and molecular genetic approaches.A theoretical molecular network for dyslexia: integrating available genetic findings.Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children.Dissection of genetic associations with language-related traits in population-based cohorts.Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations.A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.An examination of candidate gene SNPs for dyslexia in an Indian sample.Approach to epigenetic analysis in language disorders [Phonological awareness, working memory, reading and writing performances in familial dyslexia].Molecular genetics and molecular biology of dyslexia.The Influence of Dyslexia Candidate Genes on Reading Skill in Old Age A Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1

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TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

http://www.wikidata.org/entity/Q52040525

description

2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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2005年學術文章

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name

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

@en

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

@nl

type

label

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

@en

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

@nl

prefLabel

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

@en

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

@nl

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S00439-005-0017-9

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TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

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Bruce F Pennington

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Grier P Page

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Haiying Meng

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Jeffrey R Gruen

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John C DeFries

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Karl Hager

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Matthew Held

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Richard K Olson

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Shelley D Smith

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s00439-005-0017-9

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10.1007/S00439-005-0017-9

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1

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