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

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

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

http://www.wikidata.org/entity/Q33909632

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The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia Genetics of dyslexia: the evolving landscape 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 Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1.When does speech sound disorder matter for literacy? The role of disordered speech errors, co-occurring language impairment and family risk of dyslexia Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits EPHA2 is associated with age-related cortical cataract in mice and humans Language Impairments in ASD Resulting from a Failed Domestication of the Human Brain Globularity and language-readiness: generating new predictions by expanding the set of genes of interest Oral and hand movement speeds are associated with expressive language ability 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.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 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.Common variation near ROBO2 is associated with expressive vocabulary in infancy.Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment.Speaking genes or genes for speaking? Deciphering the genetics of speech and language.A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders.Etiologies and molecular mechanisms of communication disorders.Inter-relationships among behavioral markers, genes, brain and treatment in dyslexia and dysgraphia The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy.The genetics of developmental dyslexia.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 Heritability estimation for speech-sound traits with developmental trajectories.Reading skills of students with speech sound disorders at three stages of literacy development.The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains Subtyping Children With Speech Sound Disorders by Endophenotypes.Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family.The eloquent ape: genes, brains and the evolution of language.Heritability of specific language impairment depends on diagnostic criteria.Molecular windows into speech and language disorders.Association of the ROBO1 gene with reading disabilities in a family-based analysis.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.

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P2860

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

http://www.wikidata.org/entity/Q33909632

description

2004 nî lūn-bûn

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2004 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2004 թվականի հունվարին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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name

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

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

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

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

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

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

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American Journal of Human Genetics

P1476

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

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P2093

Amy Hansen

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Amy Kundtz-Kluge

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Barbara A Lewis

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Christopher Millard

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H Gerry Taylor

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James H Schick

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Karlie Russo

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Lawrence D Shriberg

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Lisa A Freebairn

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Nori Minich

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P2860

Searching for genetic determinants in the new millennium

Evidence for linkage of spelling disability to chromosome 15

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

Neural basis of an inherited speech and language disorder.

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

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

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

Quantitative trait locus for reading disability on chromosome 6

Localisation of a gene implicated in a severe speech and language disorder

A dominant gene for developmental dyslexia on chromosome 3

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283-297

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10.1086/381562

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2

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74

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Catherine M Stein

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8906097

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1181926

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