Linkage of speech sound disorder to reading disability loci. - Wikidata - wikimedia - TriplyDB

Linkage of speech sound disorder to reading disability loci.

Linkage of speech sound disorder to reading disability loci.

http://www.wikidata.org/entity/Q51988600

about

Genetic advances in the study of speech and language disorders At the height of fashion: what genetics can teach us about neurodevelopmental disabilities Gene X environment interactions in reading disability and attention-deficit/hyperactivity disorder Oral language deficits in familial dyslexia: A meta-analysis and review.Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children Association of short-term memory with a variant within DYX1C1 in developmental dyslexia Knockdown of the candidate dyslexia susceptibility gene homolog dyx1c1 in rodents: effects on auditory processing, visual attention, and cortical and thalamic anatomy.Auditory and visual sustained attention in children with speech sound disorder The genetics of reading disabilities: from phenotypes to candidate genes A multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtype.Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.A nonword repetition task for speakers with misarticulations: the Syllable Repetition Task (SRT)Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment Preschool foundations of early reading acquisition High risk of reading disability and speech sound disorder in rolandic epilepsy families: case-control study Literacy outcomes of children with early childhood speech sound disorders: impact of endophenotypes.Underlying manifestations of developmental phonological disorders in French-speaking pre-schoolers.Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.Speaking genes or genes for speaking? Deciphering the genetics of speech and language.Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders.Etiologies and molecular mechanisms of communication disorders.Annual research review: the nature and classification of reading disorders--a commentary on proposals for DSM-5.The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy.Neuropsychopathological comorbidities in learning disorders The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family.Heritability of specific language impairment depends on diagnostic criteria.Molecular windows into speech and language disorders.Early motor development is part of the resource mix for language acquisition - a commentary on Iverson's 'Developing language in a developing body: the relationship between motor development and language development'.Speech-Sound Disorders and Attention-Deficit/Hyperactivity Disorder Symptoms.Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.Speech-language pathology insights into genetics and neuroscience: beyond surface behaviour.An exploratory study of the development of early syllable structure in reading-impaired children.Prevalence of phonological disorders and phonological processes in typical and atypical phonological development.Approach to epigenetic analysis in language disorders Genome-Wide Studies of Specific Language Impairment.Speech disorder screening test for children.Communication and cognition profiles in parents of children with nonsyndromic cleft lip and/or palate.[Prevalence of speech disorders in schoolchildren and its associated factors].Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci.

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P2860

Linkage of speech sound disorder to reading disability loci.

http://www.wikidata.org/entity/Q51988600

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年學術文章

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2005年學術文章

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name

Linkage of speech sound disorder to reading disability loci.

@en

Linkage of speech sound disorder to reading disability loci.

@nl

type

label

Linkage of speech sound disorder to reading disability loci.

@en

Linkage of speech sound disorder to reading disability loci.

@nl

prefLabel

Linkage of speech sound disorder to reading disability loci.

@en

Linkage of speech sound disorder to reading disability loci.

@nl

P1433

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J.1469-7610.2005.01534.X

P1433

The Journal of Child Psychology and Psychiatry

P1476

Linkage of speech sound disorder to reading disability loci.

@en

P2093

Bruce F Pennington

http://www.w3.org/2001/XMLSchema#string

Lawrence D Shriberg

http://www.w3.org/2001/XMLSchema#string

Richard Boada

http://www.w3.org/2001/XMLSchema#string

Shelley D Smith

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P2860

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.

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

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

DeFries-Fulker multiple regression analysis of sibship QTL data: a SAS macro.

Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading.

Early reading development in children at family risk for dyslexia.

Multiple regression analysis of twin data.

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1057-1066

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10.1111/J.1469-7610.2005.01534.X

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2005-10-01T00:00:00Z

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