A dominant gene for developmental dyslexia on chromosome 3 - Wikidata - wikimedia - TriplyDB

A dominant gene for developmental dyslexia on chromosome 3

A dominant gene for developmental dyslexia on chromosome 3

http://www.wikidata.org/entity/Q28360966

about

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia Genetics of dyslexia: the evolving landscape Ocular interventions, excluding correction of significant refractive error, for specific reading disorder Ocular interventions, excluding correction of significant refractive error, for specific reading disorder The human lexinome: genes of language and reading A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1.Support for EKN1 as the susceptibility locus for dyslexia on 15q21 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 Multivariate genomewide linkage scan of neurocognitive traits and ADHD symptoms: suggestive linkage to 3q13.The genetics of reading disabilities: from phenotypes to candidate genes Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language Common variation near ROBO2 is associated with expressive vocabulary in infancy.Neuroanatomical markers for dyslexia: a review of dyslexia structural imaging studies.Converging evidence for triple word form theory in children with dyslexia.Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment Allelic variants of DYX1C1 are not associated with dyslexia in India.Identification of candidate genes for dyslexia susceptibility on chromosome 18.Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.Reading and language disorders: the importance of both quantity and quality.Use of multivariate linkage analysis for dissection of a complex cognitive trait.Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading.Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment.Comorbidity of ADHD and dyslexia.A theoretical molecular network for dyslexia: integrating available genetic findings.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.Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.Developmental dyslexia: genetic dissection of a complex cognitive trait.Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family Dissection of genetic associations with language-related traits in population-based cohorts.Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family Association 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.Longitudinal genetic analysis of early reading: The Western Reserve Reading Project.

P2860

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P2860

A dominant gene for developmental dyslexia on chromosome 3

http://www.wikidata.org/entity/Q28360966

description

2001 nî lūn-bûn

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2001 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2001 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2001年の論文

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2001年論文

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2001年論文

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2001年論文

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name

A dominant gene for developmental dyslexia on chromosome 3

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A dominant gene for developmental dyslexia on chromosome 3

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A dominant gene for developmental dyslexia on chromosome 3

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type

label

A dominant gene for developmental dyslexia on chromosome 3

@ast

A dominant gene for developmental dyslexia on chromosome 3

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A dominant gene for developmental dyslexia on chromosome 3

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prefLabel

A dominant gene for developmental dyslexia on chromosome 3

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A dominant gene for developmental dyslexia on chromosome 3

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A dominant gene for developmental dyslexia on chromosome 3

@nl

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Journal of Medical Genetics

P1476

A dominant gene for developmental dyslexia on chromosome 3

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P2093

A Voutilainen

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B Myllyluoma

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P2860

Evidence for linkage of spelling disability to chromosome 15

Quantitative-trait locus for specific language and reading deficits on chromosome 6p

Molecular cloning and functional expression of 5-HT1E-like rat and human 5-hydroxytryptamine receptor genes

Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15

Functional disruption in the organization of the brain for reading in dyslexia

A new gene (DYX3) for dyslexia is located on chromosome 2

Strategies for multilocus linkage analysis in humans

Quantitative trait locus for reading disability on chromosome 6

Dopamine D3 receptor gene: organization, transcript variants, and polymorphism associated with schizophrenia

Chromosomal localization of the human D3 dopamine receptor gene

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